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Q8IV10|Q8IV10_HUMAN
1 530 WD repeat domain 21A
WD repeat domain phosphoinositide-interacting
2 WIPI1_HUMAN 365 protein 1
>Q86XD3|
5 Q86XD3_HUMAN 521 Nucleoporin 214kDa
Q9H6U6|BCAS3_HUMAN
6 690 Breast carcinoma-amplified sequence 3
Q8WV16|WD21 A_HUMAN
7 611 WD repeat-containing protein 21A
Q8NBB8|Q8NBB8_HUMAN
8 567 cDNA FLJ33743 fis, clone BRAWH2019055
Q8WVG2|
9 Q8WVG2_HUMAN 612 WDR37 protein
10 Q2MCP6_HUMAN WDR45-like protein
11 Q17RM0_HUMAN BCAS3 protein
Q8NBB8|Q8NBB8_HUMAN
12 567 cDNA FLJ33743 fis, clone BRAWH2019055
Q8NA75|WD21C_HUMAN
13 565 WD repeat-containing protein 21C
Q8IWG1|WDR63_HUMAN
14 536 WD repeat-containing protein 63
Q8WVS4|WDR60_HUMAN
15 613 WD repeat-containing protein 60
16 WD40B_HUMAN 417 WD repeat-containing protein 40B
Q9H9M3|Q9H9M3_HUMAN
17 701 cDNA FLJ12657 fis, clone NT2RM4002140
Q8WUA4|TF3C2_HUMAN
25 608 General transcription factor 3C polypeptide 2
Q8IUW4|Q8IUW4_HUMAN
26 529 DNAI2 protein
27 PWP1_HUMAN Periodic tryptophan protein 1 homolog
Q8NCK5|Q8NCK5_HUMAN
28 572 cDNA FLJ90195 fis, clone MAMMA1001310
Q9BQ67|GRWD1_HUMAN
29 660
Q9UI46|DNAI1_HUMAN Glutamate-rich WD repeat-containing protein 1
30 746 Dynein intermediate chain 1, axonemal
cDNA FLJ75662, highly similar to Homo sapiens
31 A8K3R6_HUMAN PWP1 homolog (S. cerevisiae) (PWP1), mRNA
32 A0MNN5_HUMAN CDW4/GRWD1
cDNA FLJ76138, highly similar to Homo sapiens
WD repeat domain 78 (WDR78), transcript variant
33 A8K9W5_HUMAN 1, mRNA
34 DC1I1_HUMAN Cytoplasmic dynein 1 intermediate chain 1WD40
Q8N1S1|Q8N1S1_HUMAN cDNA FLJ37927 fis, clone CTONG2001428, weakly
35 546 similar to Xenopus laevis fizzy1 mRNA
Q8N542|Q8N542_HUMAN
36 555 DYNC1I1 protein
Q8NDM7|CJ079_HUMAN
37 575 WD repeat-containing protein C10orf79
Q8TBF7|Q8TBF7_HUMAN
38 592 DYNC1I1 protein
Q96EX3|WDR34_HUMAN
39 636 WD repeat-containing protein 34
Q9GZS0|DNAI2_HUMAN
40 683 Dynein intermediate chain 2, axonemal
Q9ULI1|Q9ULI1_HUMAN Leucine-rich repeat and WD repeat-containing
41 750 protein KIAA1239
Dynein, cytoplasmic, intermediate polypeptide
42 A4D1I7_HUMAN 1
43 A6NK54_HUMAN Uncharacterized protein WDR91
>Q7Z4X1|Q7Z4X1_HUMAN
44 508 Cytoplasmic dynein intermediate chain 2C
>Q7Z6M0|
45 Q7Z6M0_HUMAN 512 DYNC1I1 protein
Q8IY52|Q8IY52_HUMAN
46 539 DYNC1I1 protein
47 WDR32_HUMAN 367 WD repeat-containing protein 32
WD N termini
1 A8MTA5_HUMAN Uncharacterized protein SEC13
2 A8MTC1_HUMAN
3 Q4VXT1_HUMAN 285
4 WDR81_HUMAN 314 WD repeat-containing protein 81
Q9BVM5|Q9BVM5_HUMAN
5 674 WDR4 protein
6 Q6ZW40_HUMAN 495 cDNA FLJ41631 fis, clone DFNES2011499
Q8N797|Q8N797_HUMAN
7 558 CDNA FLJ25882 fis, clone CBR02655
cDNA FLJ16457 fis, clone BRAWH3009017,
8 Q6ZN41_HUMAN 488 moderately similar to SEL-10 protein
Q8TEA6|Q8TEA6_HUMAN
9 600 CDNA FLJ23731 fis, clone HEP14545
10 A6NGM1_HUMAN Uncharacterized protein EDC4
11 A6NGZ9_HUMAN Uncharacterized protein BUB3
Wd middle
Q9NXK4|Q9NXK4_HUMAN
1 730 CDNA FLJ20195 fis, clone COLF0930
WD dispersed
cDNA FLJ77982, highly similar to Homo sapiens
dynein, axonemal, intermediate polypeptide 1,
1 A8K3T1_HUMAN mRNA
Q8TEQ6|GEMI5_HUMAN
42 605 Gem-associated protein 5
Q96LY9|Q96LY9_HUMAN
43 644 cDNA FLJ32978 fis, clone TESTI2017740
Q96MR6|WDR65_HUMAN
44 646 WD repeat-containing protein 65
Q96LY9|Q96LY9_HUMAN
45 644 cDNA FLJ32978 fis, clone TESTI2017740
Q96MR6|WDR65_HUMAN
46 646 WD repeat-containing protein 65
Q96MX6|WDR92_HUMAN
47 648 WD repeat-containing protein 92
Q9BQA1|MEP50_HUMAN
48 662 Methylosome protein 50
Q9BRP4|PAAF1_HUMAN
49 664 Proteasomal ATPase-associated factor 1
Q9BUR4|WDR79_HUMAN
50 669 WD repeat-containing protein 79
Q9BV38|WDR18_HUMAN
51 671 WD repeat-containing protein 18
Q9BZH6|BRWD2_HUMAN
52 677 Bromodomain and WD repeat-containing protein 2
Q9H1Z4|WDR13_HUMAN
53 685 WD repeat-containing protein 13
Q9H977|WDR54_HUMAN
54 700 WD repeat-containing protein 54
cDNA FLJ12463 fis, clone NT2RM1000772 , weakly
Q9H9Z0|Q9H9Z0_HUMAN similar to VEGETATIBLE INCOMPATIBILITY
55 702 PROTEIN HET-E-1
Q9HCU5|PREB_HUMAN
56 711 Prolactin regulatory element-binding protein
Q9NRG9|AAAS_HUMAN
57 715 Aladin
Q9NXC5|Q9NXC5_HUMAN
58 729 CDNA FLJ20323 fis, clone HEP09648
Q9NXT1|Q9NXT1_HUMAN
59 731 CDNA FLJ20069 fis, clone COL01816
60 Q9NZJ0|DTL_HUMAN 733 Denticleless protein homolog
Q9UG25|Q9UG25_HUMAN
61 745 Putative uncharacterized protein DKFZp564A122
Q9UNY7|Q9UNY7_HUMAN
62 755 WAIT-1
63 WDR37_HUMAN 759 WD repeat-containing protein 37
64 Q53S84_HUMAN Putative uncharacterized protein DNCI2 [Fragment]
65 DMXL1_HUMAN 765 DmX-like protein 1
WD repeat domain phosphoinositide-interacting
66 WIPI2_HUMAN 768 protein 2
cDNA FLJ90410 fis, clone NT2RP3000011, weakly
Q8NC90|Q8NC90_HUMAN similar to VEGETATIBLE INCOMPATIBILITY
67 571 PROTEIN HET-E-1
Q96S15|WDR24_HUMAN
68 654 WD repeat-containing protein 24
Uncharacterized protein PAAF1(proteasomal
69 A6NDR5_HUMAN ATPase-associated factor 1)
70 A6NFL0_HUMAN Uncharacterized protein ENSP00000306791
>Q7Z6D8|
77 Q7Z6D8_HUMAN 511 Retinoblastoma binding protein 5
Q8NDZ7|Q8NDZ7_HUMAN
78 576 RBBP5 protein
Q8IWA0|WDR75_HUMAN
79 534 WD repeat-containing protein 75
80 WD42B_HUMAN WD repeat-containing protein 42B
81 A6NM93_HUMAN Uncharacterized protein MAPKBP1
82 A6NJ42_HUMAN Uncharacterized protein BUB3
Q8ND98|Q8ND98_HUMAN
83 573 Putative uncharacterized protein DKFZp434B156
84 A8K8P9_HUMAN cDNA FLJ78549
85 A6NGH5_HUMAN Uncharacterized protein WDR45
Q8N7W3|
86 Q8N7W3_HUMAN 560 cDNA FLJ40281 fis, clone TESTI2027503
87 A8MWR8_HUMAN Uncharacterized protein SEC13
>Q7LDG8|
89 Q7LDG8_HUMAN 505 Embryonic ectoderm development protein
Q8IU52|Q8IU52_HUMAN
90 528 TUWD12
91 Q4VXS9_HUMAN 283
92 Q4VXT0_HUMAN 284
Q8WUW6|
93 Q8WUW6_HUMAN 610 DMWD protein
cDNA FLJ12165 fis, clone MAMMA1000612,
Q9HA66|Q9HA66_HUMAN moderately similar to Homo sapiens G protein beta
94 703 subunit mRNA
Q9NSS8|Q9NSS8_HUMAN
95 719 Putative uncharacterized protein DKFZp434D199
96 Q96S15|WDR24_HUMAN 654
WD repeat-containing protein 24
97
Q96LM8|Q96LM8_HUMAN
98 643 CDNA FLJ25361 fis, clone TST01713
>Q86W42|THOC6_HUMAN
99 519 THO complex subunit 6 homolog
Q96RY7|IF140_HUMAN
100 653 Intraflagellar transport 140 homolog
Q96LM8|Q96LM8_HUMAN
101 643 CDNA FLJ25361 fis, clone TST01713
cDNA FLJ78749, highly similar to Homo sapiens
102 A8K8G5_HUMAN WD repeat domain 74 (WDR74), mRNA
cDNA FLJ77322, highly similar to Homo sapiens
103 A8KA70_HUMAN WD repeat domain 40A (WDR40A), mRNA
104 WDR68_HUMAN WD repeat-containing protein 68
>Q7Z4V7|Q7Z4V7_HUMAN
106 507 Protein phosphatase 2A1 B gamma subunit
Q8N5U4|Q8N5U4_HUMAN
113 557 PEX7 protein
114 WDR4_HUMAN WD repeat-containing protein 4
Q8N221|Q8N221_HUMAN
115 550 cDNA FLJ36290 fis, clone THYMU2003932
cDNA FLJ77214, highly similar to Homo sapiens
WD repeat domain 4 (WDR4), transcript variant 2,
116 A8KA58_HUMAN mRNA
Q8WUI5|Q8WUI5_HUMAN
122 609 GBL protein
123 Q6P048_HUMAN 460 WDR90 protein
124 Q6PIM1_HUMAN 470 WDFY4 protein
>Q86Y18|Q86Y18_HUMAN
126 522 LST8
Q8NEC4|Q8NEC4_HUMAN
135 577 PPP2R2C protein
Q9BRX9|MORG1_HUMAN
163 665 Mitogen-activated protein kinase organizer 1
Q9HC35|EMAL4_HUMAN
164 709 Echinoderm microtubule-associated protein-like 4
cDNA FLJ75499, highly similar to Homo sapiens
RAE1 RNA export 1 homolog (S. pombe) (RAE1),
165 A8K882_HUMAN mRNA
166 A8MV37_HUMAN Uncharacterized protein SEC13
Q96FK6|WDR89_HUMAN
167 638 WD repeat-containing protein 89
168 EIF3I_HUMAN Eukaryotic translation initiation factor 3 subunit I
Q9BVA0|KTNB1_HUMAN
186 672 Katanin p80 WD40-containing subunit B1
WD repeats only at
terminal and center Positional positinal
Analysis anal
of th
position Nuber of proteins 1
C termini 76
N termini 14 0.9 5.26%
Middle position 5
0.8 14
0.7
0.6
0.5
0.4
0.3
0.2
0.1
80.00%
0
Row 1
0.5
0.4
0.3
0.2
0.1
WD repeats which are 80.00%
dispersed through out the 0
protein Number of proteins Row 1
proteins lacking WD at N
termini 66
proteins lacking WD at
middle region 16 Positional analysis of
Protein lacking WD domain
at C termini 13 1
0.9 13.68%
0.8
0.7
0.6 16
0.5
0.4
0.3 69.47%
0.2
0.1
0
WD repeats which are Row 1
dispersed through out the
protein Number of proteins
Proteins having more WD
repeats at C termini than N
termini and middle position 131
Proteins having more WD
repeats at middle than N
termini and C-termini 20 5.63%
Proteins having more WD 12.50%
repeats at N termini than C
termini and middle position 9
81.88%
81.88%
regulation of transcription 20
cell communication 19
protein metabolism 4
cell organization 24
function analysis
37.38%
18.69%
22.43%
17.76%
3.74%
17.76%
3.74%
DOMAIN
ARCHITECTURE GENE ID N-TERMINI MIDDLE C- TERMINI
2WD WDR21A 2
2WD WIPI1 2
2WD NUP214 2
2WD 2
2WD NUP214 2
2WD BCAS3 2
2WD WDR21A 2
2WD 2
2WD WDR37 2
2WD WDR45L 2
2WD BCAS3 2
2WD WD 2
2WD 2
3WD WDR63 3
3WD WDR60 3
3WD WDR40B 3
3WD 3
3WD AAAS 3
3WD WDR63 3
3WD40 WD78 3
4WD DMWD 4
4WD WDR90 4
4WD WDR90 4
4WD 4
4WD GTF3C2 4
4WD DNAI2 4
4WD PWP1 4
4WD 4
4WD GRWD1 4
4WD 4
4WD40 PWP1 4
4(WD40) GRWD1 4
5WD WDR78 5
5WD DYNC1I1 5
5WD 5
5WD DYNC1I1 5
5WD C10orf79 5
5WD DYNC1I1 5
5WD WDR34 5
5WD DNAI2 5
5WD 5
5wd40 DYNC1I1 5
5wd wdr91 5
5WD DYNC1I2 5
5WD DYNC1I1 5
5WD DYNC1I1 5
5WD WDR32 5
5WD CDC40 5
5WD WDR76 5
5WD DYNC1I2 5
5wd40 SEC31B 5
5WD DYNC1I2 5
5WD DYNC1I2 5
5WD CDC20B 5
5WD CDC20B 5
5WD CDC20B 5
6WD WDR44 6
6WD WDR81 6
6WD WDR25 6
6WD WDR52 6
6WD 6
6WD 6
6(WD40) WDR57 6
6(WD40) WDR76 6
6(WD40) WDR24 6
6WD SCAP 6
7WD 7
7WD WDR23 7
7WD CDC20 7
7wd40 GNB5 7
7WD SPAG16 7
7WD SPAG16 7
7WD WDR42A 7
7wd40 GNB4 7
7WD PLRG1 7
9WD WDR66 9
1WD 1
1WD 1
1WD 1
1WD Wdr81 1
1WD WDR4 1
1WD 1
1WD 1
2WD 2
2WD 2
1wd40 3
3wd40 3
6wd41 NEDD8 6
7(WD40) WDR51B 7
7(WD40) WDR53 7
1WD 1
1WD 1
2WD 2
3WD NUP37 3
3WD AMBRA1 3
4wd40 DNAI1 0 2 2
6WD SCAP 0 2 4
6WD WDR25 0 4 2
4WD PREB 0 2 2
6WD 0 2 4
7WD WDR23 0 1 6
5WD SEC31B 0 2 3
6WD 0 1 5
6WD EED 0 2 4
5WD GNB5 0 2 3
12WD WDR62 0 2 10
6WD RRP9 0 1 5
6WD CSTF1 0 1 5
4WD PREB 0 2 2
5WD WDR13 0 2 3
5WD WDR13 0 2 3
5WD WDR79 0 1 4
6WD RBBP4 0 1 5
8WD AAMP 0 2 6
12WD MAPKBP1 0 2 10
12WD MAPKBP1 0 2 10
2WD NUP214 0 1 1
5WD 0 1 4
5WD 0 1 4
6WD 0 2 4
6WD WDR77 0 2 4
5WD EED 0 2 3
3WD WDR33 0 1 2
5WD 0 2 3
8WD WDR69 0 2 6
4WD WDR40C 0 1 3
12WD 0 3 9
6WD RBBP7 0 1 5
5WD DNAI2 0 2 3
8WD 0 1 7
6WD RBBP7 0 1 5
4WD 0 1 3
6WD 0 1 5
4WD WDR40A 0 1 3
5WD NUP43 0 2 3
4WD WDR20 0 1 3
12WD GEMIN5 0 3 9
2WD 0 1 2
6WD WDR65 0 1 5
2WD 0 1 2
6WD WDR65 0 1 5
4wd WDR92 0 2 2
6WD WDR77 0 3 3
6WD PAAF1 0 3 3
5WD WDR79 0 1 4
4WD WDR18 0 2 2
6WD BRWD2 0 2 4
5WD WDR13 0 1 4
3WD WDR54 0 1 2
5WD 0 1 4
4WD PREB 0 1 3
4WD AAAS 0 1 3
4WD 0 1 3
6WD 0 3 3
6WD 0 3 3
3WD 0 1 2
6WD 0 2 4
6WD 0 1 5
5wd DNCI2 0 2 3
10WD DMXL1 0 3 8
3(WD) WIPI2 0 2 1
4WD 2 0 2
6WD WDR24 WD 2 0 4
6wd40
PAAF1 3 0 3
3wd40 PPP2R2B 3 0 3
7WD STRAP 1 0 3
5WD TBL2 1 0 3
11WD WDR17 1 0 10
5WD40 2 0 3
5wd40 GTF2IRD1 2 0 3
5WD RBBP5 2 0 3
5WD RBBP5 2 0 3
5WD RBBP5 2 0 3
8WD WDR75 2 0 6
7wd40 WDR42B 3 0 4
12wd40 3 0 9
6wd 4 0 2
2WD 1 1 0
3WD 1 2 0
3wd40 2 1 0
2WD 1 1 0
3WD 2 1 0
5WD EED 2 3 0
WD EED 2 4 0
4WD WDR51B 2 2 0
2WD 1 1 0
2WD 1 1 0
2WD DMWD 1 1 0
4WD 1 3 0
2WD 1 1 0
6wD 2 4
3WD 1 1 1
3WD THOC6 1 1 1
3WD IFT140 1 1 1
3WD 1 1 1
3WD WDR74 1 1 1
4WD WDR40A 1 1 2
5WD WDR68 1 1 3
6WD PPP2R2A 1 1 4
6WD PPP2R2C 1 1 4
6WD SEC31A 1 1 4
10WD ELP2 1 1 8
12WD DMXL2 1 1 10
4WD RAE1 1 2 1
5WD AHI1 1 2 1
4WD WDR22 1 2 1
4WD PEX7 1 2 1
4WD WDR4 1 2 1
4WD 1 2 1
4WD WDR4 1 2 1
4WD RAE1 1 2 1
5WD 1 2 2
5WD WDR13 1 2 2
5WD THOC3 1 2 2
5WD 1 2 2
G protein
beta
5WD subunit-like 1 2 2
5WD WDR90 1 2 2
5WD WDFY4 1 2 2
5WD GNB2L1 1 2 2
G protein
beta
5WD subunit-like 1 2 2
5WD STXBP5 1 2 2
5WD 1 2 2
5WD GNB2 1 2 2
6WD THOC3 1 2 3
6WD WDR22 1 2 3
5WD CHAF1B 1 2 2
6WD 1 2 3
6WD WDR41 1 2 3
6WD PPP2R2C 1 2 3
6WD PEX7 1 2 3
6WD WDR82 1 2 3
6WD THOC3 1 2 3
6WD WDR22 1 2 3
6WD 1 2 3
6WD 1 2 3
6WD IFT122 1 2 3
6WD PEX7 1 2 3
7WD PPP2R2D 1 2 4
7WD GNB3 1 2 4
7WD Wdr5 1 2 4
7WD GNB1 1 2 4
7WD GNB2L1 1 2 4
7WD 1 2 4
7WD WDR48 1 2 4
7WD WDR5B 1 2 4
7WD GNB2 1 2 4
11WD WDR16 1 2 8
11WD 1 2 8
11WD WDR1 1 2 8
12WD ELP2 1 2 9
5WD 1 3 1
5WD 1 3 1
6WD GBL 1 3 2
6WD GBL 1 3 2
6WD WDR55 1 3 2
6wd40
APAF1 1 3 2
mitogen-
activated
protein
kinase
7WD organizer 1 1 3 3
9WD EML4 WD 1 3 5
4WD RAE1 2 1 1
5WD 2 1 2
5WD WDR89 2 1 2
5WD EIF3I 2 1 2
5WD MAPKBP1 2 1 2
5WD 2 1 2
5WD WDR89 2 1 2
6WD GNB1L 2 1 3
6WD TTC8 2 1 3
6WD ARPC1B 2 1 3
6WD SEC13 2 1 3
7WD IFT122 2 1 4
7WD WDR72 2 1 4
8WD WDR49 2 1 5
5WD 2 2 1
5WD 2 2 1
5wd40 ERCC8 2 2 1
6WD BUB3 2 2 2
5WD WDR19 2 2 1
6wd40
ARPC1B 2 2 2
6WD WDR53 2 2 2
6WD KATNB1 2 2 2
6wd40
ARPC1B 2 2 2
6WD NEDD1 2 2 2
7WD WDR67 2 2 3
7WD WDR61 2 2 3
7WD CIAO1 2 2 3
7WD GNB2L1 2 2 3
7WD 2 2 3
7WD WDR38 2 2 3
7WD C5orf27 2 2 3
7WD IFT122 2 2 3
7WD IFT122 2 2 3
7WD IFT122 2 2 3
7WD WDR51B 2 2 3
8WD 2 2 4
7WD WDR7 2 2 5
10WD TBL3 2 2 6
6wd40
2 3 1
5WD40 WDR7 WD 4 0 1
6WD EED 4 1 1
7WD BOP1 WD 4 2 1
5WD SEC31B 5 0 0
11WD WDR1 5 2 4
Positional
Analysis
ositional positinal
Analysis analysis
of the WD repeats
5.26%
14.74%
C termini
N terminiColumn A
Middle position
Row 1
C termini
N terminiColumn A
Middle position
Row 1
13.68%
proteins lacking WD
at N termini
16.84%
proteins lacking WD
at middle region
Protein lacking WD
domain at C termini
Row 1
5.63%
12.50%
Proteins having more
WD repeats at C
termini than N ter-
Proteins having more
WD repeats at
middle than N termini
Proteins having more
WD repeats at N
termini than C ter-
middle than N termini
Proteins having more
WD repeats at N
termini than C ter-
nalysis
cell cycle
%
regulation of
transcription
22.43% cell communication
protein metabolism
cell organization
protein metabolism
cell organization
FUNCTION
autophagy
nucleus
meiosis
Gene Ontology is not available.
Gene Ontology is not available.
nucleus
transcription
nucleus
signal transduction
cell projection organization and biogenesis
signal transduction
mRNA processing , RNA splicing
phosphoenolpyruvate-dependent sugar
phosphotransferase syste
phosphoenolpyruvate-dependent sugar
phosphotransferase syste
protein binding
nucleus
microtubule-based movement
proteolysis
function-protein binding
Biological Process
biological_process
protein binding
protein binding,
protein binding
nucleus
Gene Ontology is not available.
protein binding,histone methyltransferase activity
meiosis
cell communication
Gene Ontology is not available.
protein binding
translational initiation
nucleus
cytoplasm
lysosome
ubiquitin cycle
signal transduction , G-protein coupled receptor
protein signaling pathway
protein binding
transcription , regulation of transcription, DNA-
dependent sensory perception
, regulation of sound from RNA
of transcription
polymerase II promoter
proteolysis
phosphoenolpyruvate-dependent sugar
phosphotransferase syste
cytoplasm
Gene Ontology is not available.
cytoplasm
cytoplasm
cytoplasm
Gene Ontology is not available.
biological_process
rRNA processing , G-protein signaling, coupled to
cGMP nucleotide second messe
proteolysis
cell cycle
cell cycle
cell cycle
cell cycle
cell organization
cell cycle
transcriptin regulation
cell organization
transcriptin regulation
regulation of transcription
cell cycle
cell organization
cell organization
cell organization
cell organization
cell organization
cell organization
cell cycle
cell cycle
cell communication
cell cycle
cell organization
energy metabolism
cell cycle
cell communication
cell cycle
cell cycle
cell communication
cell organization
cell organization
cell cycle
regulation of transcription
cell organization
cell cycle
cell cycle
energy metabolism
regulation of transcription
cell cycle
transcription regulation
regulation of transcription
cell organization
cell organization
regulation of transcription
cell cycle
cell cycle
energy metabolism
energy metabolism
cell cycle
cell communication
regulation of transcription
cell cycle
cell communication
regulation of transcription
regulation of transcription
cell organization
cell organization
cell cycle
regulation of transcription
cell cycle
regulation of transcription
cell cycle
protein metabolism
cell communication
regulation of transcription
regulation of transcription
regulation of transcription
regulation of transcription
cell cycle
cell communication
cell communication
cell communication
cell cycle
regulation of transcription
cell organization
cell organization
cell communication
cell organization
cell organization
cell organization
cell cycle
cell cycle
cell comuication
cell cycle
cell communication
transcription regulation
cell cycle
cell comuication
cell communication
cell comuication
cell comuication
cell cycle
cell comuication
cell cycle
protein metabolism
cell communication
cell communication
regulation of transcription
protein metabolism
cell cycle
cell organization
energy metabolism
cell communication
cell communication
cell cycle
cell cycle
regulation of transcription
cell cycle
cell cycle
cell cycle
cell cycle
cell cycle
cell organization
transcription regulation
cell communication
cell communication
protein metabolism
cell organization
cell cycle
cell communication
description
The nuclear pore complex is a massive structure that extends across the
nuclear envelope, forming a gateway that regulates the flow of
macromolecules between the nucleus and the cytoplasm. Nucleoporins
are the main components of the nuclear pore complex in eukaryotic cells.
This gene is a member of the FG-repeat-containing nucleoporins. The
protein encoded by this gene is localized to the cytoplasmic face of the
nuclear pore complex where it is required for proper cell cycle
progression and nucleocytoplasmic transport. The 3' portion of this gene
forms a fusion gene with the DEK gene on chromosome 6 in a t(6,9)
translocation associated with acute myeloid leukemia and
myelodysplastic syndrome.
The nuclear pore complex is a massive structure that extends across the
nuclear envelope, forming a gateway that regulates the flow of
macromolecules between the nucleus and the cytoplasm. Nucleoporins
are the main components of the nuclear pore complex in eukaryotic cells.
This gene is a member of the FG-repeat-containing nucleoporins. The
protein encoded by this gene is localized to the cytoplasmic face of the
nuclear pore complex where it is required for proper cell cycle
progression and nucleocytoplasmic transport. The 3' portion of this gene
forms a fusion gene with the DEK gene on chromosome 6 in a t(6,9)
translocation associated with acute myeloid leukemia and
myelodysplastic syndrome.
0
The protein encoded by this gene is a member of a superfamily of WD
repeat proteins. The function of this protein is not yet determined;
however, other related family members perform functions involved in
regulatory processes.
The protein encoded by this gene is similar to yeast Sec31 protein. Yeast
Sec31 protein is known to be a component of the COPII protein complex
which is responsible for vesicle budding from endoplasmic reticulum
(ER). This protein was found to colocalize with SEC13, one of the other
components of COPII , in the subcellular structures corresponding to the
vesicle transport function. An immunodepletion experiment confirmed
that this protein is required for ER-Golgi transport. Alternatively spliced
transcript variants encoding distinct isoforms have been observed.
binds to the n-terminal pts2-type peroxisomal targeting signal and plays
an essential role in peroxisomal protein import.
required for 7-methylguanosine modification of trna.
0
PATHWAY
Regulation of lipid metabolism via LXR, NF-Y and SREBP,Regulation of fatty acid desaturase 2
CREB pathway,Angiotensin activation of Akt,Angiotensin activation of ERK,Angiotensin signaling via
PYK2,Angiotensin signaling via STATs,Activation of PKC via G protein coupled receptor,G-Protein
alpha-12 signaling pathway,Membrane trafficking and signal transduction of G-alpha (i) heterotrimeric
G-protein,Transcription factor Tubby signaling pathways,G-Proteins mediated regulation MARK-ERK
signaling,A2BR signaling via G-alpha-q: RSK and JNK specific pathways (map 2a),CXCR4 signaling
pathway,ICOS-ICOSL pathway in T-helper cell
a chromosomal aberration involving nup214 is found in a subset of acute myeloid leukemia (aml);
also known as acute non- lymphocytic leukemia. translocation t(6;9)(p23;q34) with dek. it results
in the formation of a dek-can fusion gene.
a chromosomal aberration involving nup214 is found in a subset of acute myeloid leukemia (aml);
also known as acute non- lymphocytic leukemia. translocation t(6;9)(p23;q34) with dek. it results
in the formation of a dek-can fusion gene.
may have a role in the development of mental symptoms in severe cases of myotonic dystrophy.
defects in ahi1 are the cause of joubert syndrome 3 (jbts3) [mim:608629]. joubert syndrome is an
autosomal recessive brain congenital malformation of the cerebellar vermis and brainstem with
abnormalities of axonal decussation (crossing in the brain) affecting the corticospinal tract and
superior cerebellar peduncles. individuals with joubert syndrome have motor and behavioral
abnormalities, including an inability to walk due to severe clumsiness and 'mirror' movements, and
cognitive and behavioral disturbances.
defects in pex7 are the cause of peroxisome biogenesis disorder complementation group 11 (pbd-
cg11) [mim:601757]. pbd refers to a group of peroxisomal disorders arising from a failure of
protein import into the peroxisomal membrane or matrix. the pbd group is comprised of four
disorders: zellweger syndrome (zws), neonatal adrenoleukodystrophy (nald), infantile refsum
disease (ird), and classical rhizomelic chondrodysplasia punctata (rcdp). zws, nald and ird are
distinct from rcdp and constitute a clinical continuum of overlapping phenotypes known as the
zellweger spectrum. the pbd group is genetically heterogeneous with at least 13 distinct genetic
groups as concluded from complementation studies.
defects in pex7 are the cause of peroxisome biogenesis disorder complementation group 11 (pbd-
cg11) [mim:601757]. pbd refers to a group of peroxisomal disorders arising from a failure of
protein import into the peroxisomal membrane or matrix. the pbd group is comprised of four
disorders: zellweger syndrome (zws), neonatal adrenoleukodystrophy (nald), infantile refsum
disease (ird), and classical rhizomelic chondrodysplasia punctata (rcdp). zws, nald and ird are
distinct from rcdp and constitute a clinical continuum of overlapping phenotypes known as the
zellweger spectrum. the pbd group is genetically heterogeneous with at least 13 distinct genetic
groups as concluded from complementation studies.
defects in pex7 are the cause of peroxisome biogenesis disorder complementation group 11 (pbd-
cg11) [mim:601757]. pbd refers to a group of peroxisomal disorders arising from a failure of
protein import into the peroxisomal membrane or matrix. the pbd group is comprised of four
disorders: zellweger syndrome (zws), neonatal adrenoleukodystrophy (nald), infantile refsum
disease (ird), and classical rhizomelic chondrodysplasia punctata (rcdp). zws, nald and ird are
distinct from rcdp and constitute a clinical continuum of overlapping phenotypes known as the
zellweger spectrum. the pbd group is genetically heterogeneous with at least 13 distinct genetic
groups as concluded from complementation studies.
A1L4B3_HUMA 1(LisH)+8(WD40)
2 N Transducin (Beta)-like 1Y-linked
A2RUS4_HUMA
3 N WD repeat domain 36 3wd+1utp
A6H8Y6_HUMA
6 N EML4 protein 1(HELP)+1wd40
A6NFH2_HUMA
7 N
A6NIN2_HUMA
10 N Uncharacterized protein EML5 3WD+1(HELP)+2wd40
A6NIY7_HUMA
11 N Uncharacterized protein TLE4 TLE_N+6wd40
cDNA FLJ76323, highly similar
A8K044_HUMA to Homo sapiens transducin
12 N (beta)-like 1X-linked, Mrna 1(LisH)+ 8wd40
A8K4K2_HUMA
17 N cDNA FLJ78025 1(LRR_1)+1wd
A8K806_HUMA
18 N cDNA FLJ77705 1wd40+1(BING4CT)
A8K9A1_HUMA
19 N cDNA FLJ77639 1wd40+1(BING4CT)
A8MSP9_HUMA
21 N Uncharacterized protein TLE4 1(TLE_N)+6wd40
Echinoderm microtubule-
22 EMAL1_HUMAN associated protein-like 1 1(HELP)+1wd40
23 WDR46_HUMAN WD repeat-containing protein 46 1WD40+1(BING4CT)
F-box/WD repeat-containing
25 FBXW4_HUMAN protein 4 1(FBOX_+4wd40
Echinoderm microtubule-
30 EMAL5_HUMAN associated protein-like 5 12WD40+1HELP+4WD40
Q4FD35_HUMA
39 N AHI1 6WD+1SH3
Q4VXZ0_HUMA
40 N WD repeat-containing protein 46 4WD+BING4CT
Q5TDG3_HUMA
42 N WD repeat domain 3 11WD+1UTP12
Q5W142_HUMA
45 N Beta-transducin repeat containing F-box+7WD
F-box/WD repeat-containing
46 FBXW9_HUMAN protein 9 F-box+6WD
Q6UX91_HUMA
52 N SQFE253 1Beach +3WD
Q86YQ0_HUMA
54 N HZGJ 1EFh+4WD
Q8IVB7|
Q8IVB7_HUMAN
55 532 Transducin (Beta)-like 3 13WD+UTP13
Q8IWB7|
WDFY1_HUMA WD repeat and FYVE domain-
56 N 535 containing protein 1 6WD+FYVE+wd
Q8N157|
AHI1_HUMAN
57 545 Jouberin 6WD+1SH3
Q8N3Y1|
FBXW8_HUMAN F-box/WD repeat-containing
58 554 protein 8 F-BOX+6WD
Q8N5D0|
WDTC1_HUMA WD and tetratricopeptide repeats
59 N 556 protein 1 6WD+1TPR_1
Q8NAA4|
Q8NAA4_HUMA
60 N 566 Autophagy-related protein 16-2 ATG16+7WD
>Q8TED0|
UTP15_HUMAN U3 small nucleolar RNA- 6WD+U3 small nucleolar
62 602 associated protein 15 homolog RNA C terminal
Q92828|
COR2A_HUMAN
63 620 Coronin-2A 4WD+DUF1900
Q969H0|
FBXW7_HUMAN F-box/WD repeat-containing
64 621 protein 7 8WD+FBOX
Q969U6|
FBXW5_HUMAN F-box/WD repeat-containing
65 622 protein 5 3WD+FBOX
Q96A78|
Q96A78_HUMA
66 N 625 TBL3 protein 13WD+UTP13
Q96LK4|
Q96LK4_HUMA CDNA FLJ25420 fis, clone
68 N 642 TST03665 2WD+FYVE+1WD
Q96P52|
Q96P52_HUMAN WD40-and FYVE-domain
69 649 containing protein 3 4WD+FYVE
Q96P53|
WDFY2_HUMA WD repeat and FYVE domain-
70 N 650 containing protein 2 5WD+FYVE
Q99698|
LYST_HUMAN
71 658 Lysosomal-trafficking regulator 4WD+BEACH
Q9BQ87|
TBL1Y_HUMAN F-box-like/WD repeat-containing
72 661 protein TBL1Y 8WD+LiSH
Q9NRL3|
STRN4_HUMAN
76 717 Striatin-4 7WD+STRIATIN
Q9NV06|
SOF1_HUMAN WD repeat and SOF domain-
77 721 containing protein 1 5WD+SOF1
Q9NVX2|
NLE1_HUMAN
78 724 Notchless protein homolog 1 8WD+NLE
Q9NWG8|
Q9NWG8_HUMA cDNA FLJ10035 fis, clone
79 N 726 HEMBA1000919 2WD+ATG16
Q9NYS7|
WSB2_HUMAN WD repeat and SOCS box-
80 732 containing protein 2 6WD+SOCS
Q9P0U0|
Q9P0U0_HUMA
81 N 734 PC326 protein 2WD+IQ
Q9UKB1|
FBW1B_HUMAN F-box/WD repeat-containing
82 648 protein 11 7WD+FBOX
Q9UKT8|
FBXW2_HUMAN F-box/WD repeat-containing
83 749 protein 2 5WD+FBOX
Q9ULV4|
COR1C_HUMAN
84 751 Coronin-1C 3WD+DUF1900
Q9UNX4|
WDR3_HUMAN
85 754 WD repeat-containing protein 3 10WD+UTP12
STB5L_HUMAN
87 760 Syntaxin-binding protein 5-like LLGL+6WD
Q9C0J8|
WDR33_HUMAN
90 681 WD repeat-containing protein 33 6WD+COLLAGEN
Q9H2Y7|
ZF106_HUMAN
91 687 Zinc finger protein 106 homolog 6WD+1ZnF_C2H2
Q9UFC0|
LRWD1_HUMAN Leucine-rich repeat and WD
92 740 repeat-containing protein 1 1WD+1LRR
94 Q8TBC3|SHKB1_HUMANSH3KBP1-binding
591 protein 1 1btb+1wd
WD repeat-containing protein
Q8NI36|WDR36_HUMAN 586 36 Utp21
wd+2
A5YM44_HUMA
1 N
Lipopolysaccharide-responsive
5 LRBA_HUMAN and beige-like anchor protein 1DUF1088+1Beach+5wd40
Q5T3M3_HUMA
9 N Tubby like protein 4 2WD+SOCS _BOX+TUB
7( WD40)+1(
Coatomer_WDAD)+1
10 COPA_HUMAN Coatomer subunit alpha COPI_C
Q17RK4_HUMA 4WD+1DUF1900+3WD+1D
11 N Coronin 7 UF1900
Q86TI4| 4WD+1PQQ+1WD+1PQQ+
12 Q86TI4_HUMAN WD repeat-containing protein 86 1WD
Q8IZQ1|
WDFY3_HUMA WD repeat and FYVE domain-
14 N 540 containing protein 3 1BEACH+5WD+1FYVE
Q8N9V3|
WSDU1_HUMA WD repeat, SAM and U-box
15 N 563 domain-containing protein 1 7WD+SAM+UBOX
Q8WWQ0|
PHIP_HUMAN
16 614 PH-interacting protein 8WD+2BROMO
Q92636|
FAN_HUMAN
17 618 Protein FAN 1GRAM+1BEACH+7WD
Q9H7D7|
WDR26_HUMAN
18 692 WD repeat-containing protein 26 5WD+CTLH+LisH
Q9NRJ4|
TULP4_HUMAN
19 716 Tubby-related protein 4 1WD+SOCS+TUB
Q9NSI6|
BRWD1_HUMA Bromodomain and WD repeat-
20 N 718 containing protein 1 6WD+2BROMO
A8K194_HUMA 3(wd40)+1(HIRA_B)+1(Hira
22 N )
E3 ubiquitin-protein ligase
23 TRAF7_HUMAN TRAF7 1RING+1zf-TRAF+7WD
cDNA FLJ75683, highly similar
to Homo sapiens TAF5 RNA
polymerase II, TATA box
A8K5B4_HUMA binding protein (TBP)-associated 1LISH+1(TFIID_90kDa)+6w
24 N factor, 100kDa (TAF5), mRNA d40
Q5T3M2_HUMA
26 N Tubby like protein 4 2WD+1SOCS+2WD+TUB
CORO6_HUMAN
31 478 Coronin-6 DUF1899+3WD+1DUF1900
Q9UQ03|
COR2B_HUMAN
32 756 Coronin-2B DUF1899+4WD+1DUF1900
Q9BR76|
COR1B_HUMAN
33 663 Coronin-1B DUF1899+3WD+1DUF1900
4WD+1DUF1900+3WD+1D
34 CORO7_HUMAN Coronin-7 UF1900
Leucine-rich repeat
35 LRRK2_HUMAN serine/threonine-protein kinase 2 Miro+Pkinase+1WD
wd+3
Phosphoinositide-3-kinase,
1 A0JP11_HUMAN regulatory subunit 4, p150 1STYKc+2HEAT+6WD
Q99570|
PI3R4_HUMAN Phosphoinositide 3-kinase
2 656 regulatory subunit 4 6WD+S_TKC+2HEAT
Q8N122|
RPTOR_HUMAN Regulatory-associated protein of
3 543 mTOR 7WD+3HEAT
wd+6
A0AUV9_HUMA 4(TEP1_N)+1(TROVE)+1(N
1 N Telomerase-associated protein 1 ACHT)+18(wd)
wd+7
Uncharacterized protein
1 K0329_HUMAN KIAA0329/KIAA0297 10(TECPR)+3wd40
wd+11
Q17RV3_HUMA 8(LRR)+1LRR_TYP+1small
1 N Leucine-rich repeat kinase 2 _GTPase +1STYKc+1WD40
40.00%
45.26%
14.74%
40.00%
tethered domain present in
middle 14
40.00%
positional analysis of WD
domain in wd+2 tethered Number of
population proteins
26.67%
tethered domain present in N
terminal 6
tethered domain present in
midle 4
tethered domain present in C
terminal 5
33.33%
positional analysis of WD
domain in wd+2 tethered Number of positional analysis of tethered domain i
population proteins
tethered domain lack in N 25.00%
terminal 5
tethered domain lack in middle 13
tethered domain lack in C 10
terminal 2
65.00%
wd+3
tethered domains lack in C
terminal 2
tethered domains present only
in middle 1
wd+6
tethered domains lack in C
terminal 2
wd+7
tethered domains lack in
middle 1
wd+10
tethered domains lack in
Middle 1
wd+11
tethered domains lack in N
terminal 1
previous
Ubiquitin associated 19
Cell Cycle of
Regulation 3
transcription 24
autophagy 3
Cell organization 1
Apoptosis 3
Protein Transport 10
WNT signaling 12
Notch signalling 1
76
25
22.5
20
number of protein
17.5
15
12.5
10
7.5 Column B
5
2.5
0
Ubi- Cell Regu- auto- Cell Apop- Pro- WNT Notch
quitin Cycle lation phagy organ- tosis tein signal- sig-
asso- of ization Trans ing nalling
process involved
sir's
Ubiquitn Associated 11
Cell Cycle 2
Regulation of transcription 17
autophagy 3
Cell organization 1
Apoptosis 4
Protein Transport 9
WNT signaling 10
Notch signalling 1
gene id n-termini middle c-termini
STRN3 Striatin 1 0 0
wd 0 0 5
TBL1Y LisH 1 0 0
wd 0 1 7
WDR36 wd 2 0 1
utp 0 0 1
ATG16L1 ATG16 1 0 0
WD 0 0 6
ATG16L1 ATG16 1 0 0
WD 1 1 4
EML4 HELP 1 0 0
WD 0 0 1
TLE1 TLE_N 1 0 0
WD 0 0 6
NBEAL1 BEACH 0 0 1
WD 0 0 2
STRN3 Striatin 1 0 0
WD 0 0 5
EML5 HELP 0 0 1
WD 3 0 2
TLE4 TLE_N 1 0 0
WD 0 0 6
TBL1X LISH 1 0 0
WD 2 1 5
FBXW8 F-BOX 1 0 0
WD 0 0 1
BOP1 BOPOINT 1 0 0
WD 0 0 2
TLE1 TLE_N 1 0 0
WD 0 0 6
no terms found WD 0 0 1
BING4CT 0 0 1
no terms found WD 4 0 0
HMG 0 0 1
TLE4 TLE_N 1 0 0
WD 0 0 6
EML1 HELP 1 0 0
WD 0 0 1
WDR46 WD 0 0 1
BING4CT 0 0 1
PRPF4 SFM 1 0 0
WD 1 0 6
FBXW4 FBOX 1 0 0
WD 1 1 2
TLE1 TLE_N 1 0 0
WD 0 1 5
TLE2 TLE_N 1 0 0
WD 0 0 6
TLE3 TLE_N 1 0 0
WD 0 0 6
TLE4 TLE_N 1 0 0
WD 0 0 6
EML5 WD 10 1 5
HELP 0 0 1
STRN3 striatin 0 1 0
wd 0 0 7
BOP1 BOP1NT 0 1 0
WD 0 0 7
NWD1 nacht 0 0 1
wd 0 0 11
STXBP5 LLGL 1 0 0
WD 7 0 0
WDR43 NUC189 0 0 1
WD 1 2 2
PWP2 PWP2 0 0 1
WD 0 3 10
KIF21A KISC 1 0 0
WD 0 0 7
EML3 HELP 1 0 0
WD 1 3 4
AHI1 SH3 0 0 1
WD 0 6 0
WDR46 BING4CT 0 0 1
WD 0 2 2
STXBP5 LLGL 1 0 0
WD 7 0 0
WDR3 UTP12 0 0 1
WD 4 3 4
TAF5L TFIID_90kDa 0 1 0
WD 0 0 1
TAF5L TFIID_90kDa 0 1 0
WD 0 0 6
BTRC F-BOX 0 1 0
WD 0 2 5
FBXW9 F-BOX 0 1 0
WD 0 3 3
ATG16L1 ATG16 1 0 0
WD 0 2 5
DKFZp686K03100 BEACH 0 1 0
WD 0 0 5
DKFZp781N011 F-BOX 0 1 0
WD 0 2 5
PRPF4 SFM 0 1 0
WD 0 2 5
TLE3 TLE_N 1 0 0
WD 0 0 7
NBEAL2 BEACH 0 1
WD 0 0 3
NBEAL1 BEACH 0 0 1
WD 0 0 3
HZGJ Efh 1 0 0
WD 0 0 4
TBL1Y WD 13 0 0
UTP13 0 0 1
WDFY1 WD 6 0 1
FYVE 0 0 1
AHI1 WD 0 0 6
SH3 0 0 1
FBXW8 F-BOX 1 0 0
WD 0 0 6
WDTC1 WD 4 0 2
TPR_1 0 1 0
ATG16L2 ATG16 1 0 0
WD 0 0 7
0
WD 0 0 6
SOCS 0 0 1
UTP15 WD 6 0 0
U3 small
nucleolar RNA
C terminal 0 0 1
CORO2A WD 4 0 0
DUF1900 0 1 0
FBXW7 WD 0 0 8
FBOX 1
FBXW5 WD 1 0 2
FBOX 1
TBL3 WD 4 5 4
UTP13 0 0 1
PPWD1 WD 2 2 0
PRO_ISOMER
ASE 0 0 1
WD 2 0 1
FYVE 0 0 1
WDFY3 WD 3 0 1
FYVE 0 0 1
WDFY2 WD 2 2 1
FYVE 0 0 1
LYST WD 0 0 4
BEACH 0 0 1
TBL1Y WD 0 0 8
LiSH 1 0 0
WD 3 2 0
SH3 1 1
WD 0 0 2
TPR_1 1 0 0
WD 5 0 1
FYVE 0 0 1
STRN4 WD 0 0 7
STRIATIN 1 0 0
WDSOF1 WD 2 1 2
SOF1 0 0 1
NLE1 WD 0 0 8
NLE 1 0 0
WD 0 0 2
ATG16 1 0 0
WSB2 WD 1 0 5
SOCS 0 0 1
IQWD1 WD 0 0 2
IQ 0 0 1
FBXW11 WD 0 0 7
FBOX 1 0 0
FBXW2 WD 0 0 5
FBOX 1 0 0
CORO1C WD 3 0 0
DUF1900 0 0 1
WDR3 WD 3 0 7
UTP12 0 0 1
BTRC WD 0 0 6
FBOX 0 1 0
STXBP5L WD 2 4 0
LLGL 1 0 0
WSB1 WD 0 0 6
SOCS 0 0 1
0
KIF21B KISC 1 0 0
WD 0 0 7
WDR33 WD 0 0 6
COLLAGEN 0 1 0
ZFP106 WD 0 0 6
ZnF_C2H2 0 0 1
LRWD1 LRR 1 0 0
WD 0 0 1
BRWD3 WD 8 0 0
BROMO 0 0 1
SHKBP1 BTB 1 0 0
wd 0 1 2
WDR36 Utp21 0 0 1
WD40 5 0 3
APAF1 CARD 1 0 0
NB-ARC 1 0 0
WD 0 6 6
APAF1 CARD 1 0 0
NB-ARC 1 0 0
WD 0 7 6
PHIP BROMO 0 0 2
WD 8 0 0
NSMAF GRAM 0 1 0
BEACH 0 1 0
WD 0 0 7
LRBA DUF1088 0 0 1
BEACH 0 0 1
WD 0 0 5
HIRA WD 7 0 0
HIRA_B 0 1 0
HIRA 0 0 1
TAF5 LISH 1 0 0
TFIID_90kDa 1 0 0
WD 0 0 6
SMU1 LISH 1 0 0
CTLH 1 0 0
WD 0 2 5
TULP4 WD 2 0 0
SOCS 1 0 0
TUB 0 0 1
WD 0 0 6
COPA WD 7 0 0
coatomer_WD
AD 0 1 0
COPI_C 0 0 1
CORO7 WD 4 0 3
DUF1900 1 0 1
WDR86 WD 1 3 2
PQQ 0 0 2
NSMAF GRAM 0 1 0
BEACH 0 1 0
WD 0 0 7
WDFY3 BEACH 0 0 1
WD 0 0 5
FYVE 0 0 1
WDSUB1 WD 4 3 0
SAM 0 0 1
UBOX 0 0 1
PHIP WD 8 0 0
BROMO 0 0 2
NSMAF GRAM 0 1 0
BEACH 0 1 0
WD 0 0 7
WDR26 WD 0 0 5
CTLH 0 1 0
LisH 1 0 0
TULP4 WD 1 0 0
SOCS 1 0 0
TUB 0 0 1
BRWD1 BROMO 0 1 1
WD 6 0 0
DDR1 HELP 1 0 0
WD 1 0 0
Pkinase_Tyr 0 0 1
HIRA wd 3 0 0
HIRA_B 0 1 0
hira 0 0 1
TRAF7 RING 1 0 0
zf-TRAF 0 1 0
WD 0 0 7
TAF5 LISH 1 0 0
TFIID_90kDa 1 0 0
WD 0 0 6
WDR33 COLLAGEN 0 1 0
RPT 0 1 0
WD 7 0 0
TULP4 SOCS 0 1 0
TUB 0 0 1
WD 2 2 0
CORO1C DUF1900 0 0 1
WD 3 0 0
DUF1899 1 0 0
DUF1900 0 0 1
WD 4 0 0
DUF1899 1 0 0
CORO1A WD 3 0 0
DUF1900 0 0 `1
DUF1899 1 0 0
CORO2A WD 4 0 0
DUF1900 0 0 1
DUF1899 1
CORO6 WD 3 0 0
DUF1900 0 0 1
DUF1899 1 0 0
CORO2B WD 4 0 0
DUF1900 0 0 1
DUF1899 1 0 0
CORO1B WD 3 0 0
DUF1900 0 0 1
DUF1899 1
CORO7 WD 4 0 3
DUF1900 1 0 1
LRRK2 miro 1 0 0
pkinase 0 0 1
WD 0 0 1
PIK3R4 STYKc 1 0 0
HAET 0 2 0
WD 0 0 6
PIK3R4 HEAT 0 2 0
S_TKC 1 0 0
wd 0 0 6
KIAA1303 wd 0 0 7
HEAT 0 3 0
TEP1 tep1 4 0 0
trove 1 0 0
nacht 0 1 0
wd 0 0 18
TEP1 tep1 4 0 0
trove 1 0 0
nacht 0 1 0
wd 0 0 12
HERC5 RCC1 2 0 4
SPRY 0 1 0
HECT 0 0 1
wd40 0 0 6
KIAA0329 TECPR 2 0 8
wd 3 0 0
LRRK2 LRR 0 8 0
LRR_TYP 0 1 0
small_GTPase 0 0 1
wd 0 0 1
STYKc 0 0 1
40.00%
45.26% tethered domain present in N
terminal
tethered domain present in
middle
tethered domains present in
c terminal
40.00%
40.00%
tethered domain
present in N terminal
tethered domain
present in midle
tethered domain
present in C terminal
33.33%
25.00%
Cell Cycle 21
Regulation of transcription 22
Cell organization 13
Protein metabolism 1
cell communication 17
86
functional analysis in tethered population
24.42%
13.95%
25.58%
19.77%
15.12% 1.16%
Column B
functions tethering number
Cell cycle 1
rRNA processing,visual
perception,biological_processes,response to
stimulus 1 1ERJ 7
proteolysis 1
transcription,transduction,regulation of
transcription,DNA dependent signal
transduction,multicellular organismal
development,organ morphogenesis,wnt receptor
signalling pathway,negative regulation of
transcription,negative regulation of wnt receptor
signalling pathway,regulation of transcription 1 1GXR 7
not available 1
Cell cycle 1
not available 1
regulation of transcription 1
1
transcription,transduction,regulation of
transcription,DNA dependent signal
transduction,multicellular organismal
development,organ morphogenesis,wnt receptor
signalling pathway,negative regulation of
transcription,negative regulation of wnt receptor
signalling pathway,regulation of transcription 1 1GXR 7
visual perception 1
translation,tRNA aminoacylation for protein
translation,biological_process,biosynthetic process 1
not found 1
cell cycle 1
no function 1
microtubule-based movement 1
rRNA processing 1
ubiquitin cycle 1
binding(mol function) 1
no results 1
binding 1
rRNA processing
1
glutamine biosynthetic process , nitrogen
compound metabolic process , intracellular
signaling cascade
1
ubiquitin cycle 1
1
binding , zinc ion binding , metal ion binding
1
rRNA processing
1
ubiquitin-dependent protein catabolic process ,
ubiquitin cycle , signal transduction , Wnt
receptor signaling pathway 1
postreplication repair,transport,phosphate
transport,spermatogenesis 1
protein binding 1
nucleus , cytoplasm 2
electron transport 2
2
MAPKKK cascade , protein amino acid
phosphorylation , small GTPase mediated signal
transduction , positive regulation of protein
ubiquitination , positive regulation of
programmed cell death , protein amino acid
autophosphorylation
binding 1
Ubiquitn Associated
24.42% Cell Cycle
13.95% Regulation of
transcription
19.77%
Cell organization
Protein metabolism
1.16% cell communication
process
cell cycle
cell organization
cell cycle
cell cycle
protein metabolism
regulation of transcription
cell cycle
regulation of transcription
regulation of transcription
regulation of transcription
cell communication
cell organization
cell organization
ubiquitin cycle
regulation of transcription
regulation of transcription
regulation of transcription
regulation of transcription
cell organization
cell communication
cell organization
cell organization
cell organization
regulation of transcription
regulation of transcription
cell communication
ubiquitin cycle
cell cycle
cell organization
regulation of transcription
cell communication
ubiquitin cycle
ubiquitin cycle
regulation of transcription
cell organization
regulation of transcription/ubiquitin cycle
cell communication
cell organization
cell comunication
ubiquitin cycle
cell communication
ubiquitin cycle
ubiquitin cycle
cell communication
cell organization
ubiquitin cycle
cell cycle
ubiquitin cycle
cell cycle
cell cycle
regulation of ranscription
cell cycle
cell cycle
cell communication
cell communication
cell organization
regulation of transcription
regulation of transcription
cell cycle
cell cycle
cell communication
ubiquitin cycle
cell communication
cell communication
cell communication
regulation of transcription
cell communication
cell cycle
cell communication
cell cycle
cell communication
cell cycle
cell cycle
ubiquitin cycle
cell cycle
cell cycle
cell cycle
cell cycle
Ubiquitin cycle
cell communication
description
required for maturation of the 25s and 5.8s ribosomal rnas. required for
proper processing at four distinct sites located within the internal transcribed
spacers its1 and its2 and the 3' external spacer. may serve as an essential
factor in ribosome formation that coordinates processing of the spacer
regions in pre-rrna (by similarity).
Syntaxin 1 is a component of the 7S and 20S SNARE complexes which are
involved in docking and fusion of synaptic vesicles with the presynaptic
plasma membrane. This gene encodes a syntaxin 1 binding protein. In rat, a
similar protein dissociates syntaxin 1 from the Munc18/n-Sec1/rbSec1
complex to form a 10S complex, an intermediate which can be converted to
the 7S SNARE complex. Thus this protein is thought to be involved in
neurotransmitter release by stimulating SNARE complex formation.
Alternatively spliced variants have been identified, but their biological
validity has not been determined.
This gene encodes a protein that contains two WD domains and an FYVE
zinc finger region. The function of this gene is unknown. An alternatively
spliced transcript variant of this gene may exist.
the coatomer is a cytosolic protein complex that binds to dilysine motifs and
reversibly associates with golgi non- clathrin-coated vesicles, which further
mediate biosynthetic protein transport from the er, via the golgi up to the
trans golgi network. coatomer complex is required for budding from golgi
membranes, and is essential for the retrograde golgi-to-er transport of
dilysine-tagged proteins. in mammals, the coatomer can only be recruited by
membranes associated to adp-ribosylation factors (arfs), which are small gtp-
binding proteins; the complex also influences the golgi structural integrity,
as well as the processing, activity, and endocytic recycling of ldl receptors
(by similarity).
may be involved in cell-cell interactions and recognition.
Number of domains
ZnF_C2H2 1 22.5 6
DUF1088 1 20 7
coatomer_WDAD 1 8
COPI_C 1 17.5 9
PQQ 1 15 10
SAM 1 11
UBOX 1 12.5
Pkinase_Tyr 1 10
S_TKC 1
tep1 1 7.5
trove 1
5
RCC1 1
HECT 1 2.5
SPRY 1
0
TECPR 1
1 2 3 4 5
LRR_TYP 1
DUF1899 1 Appeare
BTB 1
MIRO 1
UTP21 1
EFH 1
small_GTPase 1
SFM 2
KISC 2
COLLAGEN 2
STYKc 2
UTP12 2
RING 2
UTP13 2
TPR_1 2
CARD 2
HIRA_B 2
HIRA 2
CTLH 2
NB-ARC 2
nacht 3
LLGL 3
SH3 3
LRR 3 sl.no
TUB 3 1
GRAM 3 2
HEAT 3 3
striatin 4 4
TFIID_90kDa 4 5
BING4CT 4 6
BROMO 4 7
ATG16 5 8
HELP 6
SOCS 7
FYVE 6 tethered frequency o
Fbox 6
lish 8 350
TLE_N 9
300
BEACH 10
Number of proteins
DUF1900 11 250
150
100
50
0
Wd wd+1 wd+2 wd+3 wd+6
Domain tethered in Pr
WD sociality
Analysis of Domain occurence
No of TIMES OF DOMAIN
OCCURING IN THE
POPULATION
34
13
7
4
1
3
1
1
1
1
1
2 3 4 5 6 7 8 9 10 11
Appearence frequency
number of tethered domain number of proteins
Wd 303
wd+1 95
wd+2 35
wd+3 3
wd+6 2
wd+7 1
wd+10 1
wd+11 1
441
Column G
WD sociality
Wd
wd+1
wd+2
wd+3
wd+6
wd+7
wd+10
wd+11
wd+7
wd+10
wd+11
Saccharomyces cerevisiae
Fungi
Caenorhabditis elegans
Nematoda (roundworms)
Metazoa
Drosophila melanogaster (Fruit fly)
Arthropoda
Chordata
Mus musculus (Mouse)
Homo sapiens (Human)
Eukaryota
Viruses
Archaea
Bacteria
Cyanobacteria
Synechocystis sp. (strain PCC 6803)
Oryza sativa (Rice)
Arabidopsis thaliana (Mouse-ear cress)
Viridiplantae(green plants)
plastid group
other eukaryotes
204
3972
171
477
4970
319
971
3108 species wide distribution of WD Proteins
670
718
15126
17
55 16000
909
261 15000
Saccharomyces
8 species wide distribution of wd proteins
14000 cerevisiae
811
443 13000 Fungi
2661 Caenorhabditis elegans
5225
12000 Nematoda (roundworms)
779 11000 Metazoa
10000 Drosophila melanogaster
(Fruit fly)
9000 Arthropoda
8000 Chordata
7000 Mus musculus (Mouse)
Homo sapiens (Human)
6000
Eukaryota
5000 Viruses
4000 Archaea
3000 Bacteria
Cyanobacteria
2000
Synechocystis sp. (strain
1000 PCC 6803)
0
Column H
Homo sapiens (Human)
6000
Eukaryota
5000 Viruses
4000 Archaea
3000 Bacteria
Cyanobacteria
2000
Synechocystis sp. (strain
1000 PCC 6803)
0
Column H
species
WD Proteins
Guanine nucleotide-
binding protein subunit
1 GBB5_HUMAN beta-5 5WD GNB5
Histone-binding protein
2 RBBP7_HUMAN RBBP7 6WD RBBP7
Q6FHM2_HUMAN
4 447 GNB2 protein 5WD GNB2
5 A5YM44_HUMAN APAF1
FUNCTION process description
1.CREB pathway,Angiotensin activation of Akt,Angiotensin activation of ERK,Angiotensin signaling via PYK2,Angiotensin signaling via
STATs,Activation of PKC via G protein coupled receptor,G-Protein alpha-12 signaling pathway,G-protein families signaling pathway,Membrane
trafficking and signal transduction of G-alpha (i) heterotrimeric G-protein,Transcription factor Tubby signaling pathways,G-Proteins mediated
regulation MARK-ERK signaling,ChREBP regulation pathway,Rhodopsin phototransduction cascade in retina - the key role of Ca2+
transport,Putative erythropoietin signaling pathway (part 2),A2BR signaling via G-protein beta/gamma dimer. Activation of PI3K, PLCB and
PLA2,A2BR signaling via G-beta/gamma dimer. Activation of PH-domain proteins. (map 1),A2BR signaling via G-beta/gamma dimer. RGS and
CaM-related GIRK regulation,A2BR signaling via G-beta/gamma dimer. Activation of PH-domain proteins. (map 2),A2BR signaling via G-alpha-q:
Inhibition of TKR-specific PI3K activation (map 1a),A2BR signaling via G-alpha-q: Inhibition of TKR-specific PI3K activation (map 1b),A2BR
signaling via G-alpha-q: RSK and JNK specific pathways (map 2a),A2BR signaling via G-alpha-q: PRKCA - RSK & JNK specific pathways (map
2b),A2BR signaling via G-alpha-q: PRKCA - RSK & JNK specific pathways (map 2c),A2BR signaling via G-alpha-q: PRKCB/G/Q specific
pathways (map 3a),A2BR signaling via G-alpha-q: PRKCE - RASGRP specific pathways (map 3b),Regulation of fatty acid metabolic enzymes
FACL, ACADM, FASN and SCD via adenosin receptor activation, Angiotensin signaling via beta-arrestin,Calcium signaling,IP3 signaling,CXCR4
signaling pathway,ICOS-ICOSL pathway in T-helper cell,G-Protein alpha-i signaling cascades,G-Protein alpha-q signaling cascades,G-Protein
alpha-s signaling cascades,G-Protein beta/gamma signaling cascades,PDGF signaling via MAPK cascades, cAMP signaling,BAD
phosphorylation,Ceramide-dependent NO antiapoptotic action, PKA signaling,PIP3 signaling in cardiac myocytes,PIP3 signaling in B lymphocytes
CREB pathway,Angiotensin activation of Akt,Angiotensin activation of ERK,Angiotensin signaling via PYK2,Angiotensin signaling via
STATs,Activation of PKC via G protein coupled receptor,G-Protein alpha-12 signaling pathway,G-protein families signaling
Ligand-Dependent
pathway,Membrane Transcription of Retinoid-Target
trafficking and genes,P53
signal transduction signaling
of G-alpha pathway,Estrogen
(i) heterotrimeric receptor signaling
G-protein,Transcription pathway,ATM-H2AX-
factor Tubby signaling
NFBD1 DNA damage
pathways,G-Proteins response,Role
mediated of heterochromatin
regulation protein 1 (HP1)regulation
MARK-ERK signaling,ChREBP family in transcriptional silencing,,Formation
pathway,Rhodopsin of Sin3A
phototransduction and in
cascade
NuRD complexes and their role in transcription regulation
retina - the key role of Ca2+ transport,Putative erythropoietin signaling pathway (part 2),A2B receptor: action via G-protein alpha s
(map 1),A2BR signaling via G-protein beta/gamma dimer. Activation of PI3K, PLCB and PLA2,A2BR signaling via G-beta/gamma
dimer. RGS and CaM-related GIRK regulation,A2BR signaling via G-beta/gamma dimer. Activation of PH-domain proteins. (map
2),A2B Receptor: Action via G-alpha s. (map 2),A2BR signaling via G-alpha-q: Inhibition of TKR-specific PI3K activation (map
1a),A2BR signaling via G-beta/gamma dimer. Activation of PH-domain proteins. (map 1),A2B Receptor: Action via G-alpha s. (map
2),A2BR signaling via G-alpha-q: Inhibition of TKR-specific PI3K activation (map 1a),A2BR signaling via G-alpha-q: Inhibition of TKR-
specific PI3K activation (map 1b),A2BR signaling via G-alpha-q: Inhibition of TKR-specific PI3K activation (map 1b),A2BR signaling via
G-alpha-q: PRKCA - RSK & JNK specific pathways (map 2c),A2BR signaling via G-alpha-q: PRKCB/G/Q specific pathways (map
3a),A2BR signaling via G-alpha-q: PRKCE - RASGRP specific pathways (map 3b),Regulation of fatty acid metabolic enzymes FACL,
ACADM, FASN and SCD via adenosin receptor activation,Angiotensin signaling via beta-arrestin,Calcium signaling,IP3
signaling,CXCR4 signaling pathway,ICOS-ICOSL pathway in T-helper cell,G-Protein alpha-i signaling cascades,G-Protein alpha-q
signaling cascades,G-Protein alpha-s signaling cascades,G-Protein beta/gamma signaling cascades,PDGF signaling via MAPK
cascades,cAMP signaling,cAMP signaling,Ceramide-dependent NO antiapoptotic action,PKA signaling,PIP3 signaling in cardiac
myocytes,PIP3 signaling in B lymphocytes
p53-dependent apoptosis,Cytoplasm/mitochondrial transport of proapoptotic proteins Bid, Bmf and Bim,Regulation of apoptosis by mitochondrial
proteins,Caspases cascade
G-protein adaptor/regulatory :beta/gamma
A6NFH2_HUM
1 AN TLE1 TLE_N 1
WD 0
cDNA FLJ76330,
highly similar to Homo
sapiens F-box and WD-
40 domain protein 8
A8K0Q6_HUM (FBXW8), transcript
2 AN variant 2, mRNA 1(F-box)+1wd40 FBXW8 F-BOX 1
cDNA FLJ76273,
highly similar to Homo
sapiens transducin-like
enhancer of split 1
(E(sp1) homolog,
A8K495_HUM Drosophila) (TLE1),
3 AN mRNA 1(TLE_N)+6wd40 TLE1 TLE_N 1
Transducin-like
6 TLE1_HUMAN enhancer protein 1 1TLE_N+6wd40 TLE1 TLE_N 1
WD 0
Transducin-like
7 TLE2_HUMAN enhancer protein 2 1TLE_N+6wd40 TLE2 TLE_N 1
WD 0
Transducin-like
8 TLE3_HUMAN enhancer protein 3 1TLE_N+2wd40 TLE3 TLE_N 1
WD 0
Transducin-like
9 TLE4_HUMAN enhancer protein 4 1TLE_N+2wd40 TLE4 TLE_N 1
WD 0
TAF5-like RNA
polymerase II,
p300/CBP-associated
factor (PCAF)-
Q5TDI5_HUM associated factor, 1TFIID_90kDa+1W TFIID_90k
10 AN 65kDa D TAF5L Da 0
WD 0
Q6PI57_HUM
12 AN TLE3 protein TLE_N +7WD TLE3 TLE_N 1
WD 0
Q96A78|
Q96A78_HUM
13 AN 625 TBL3 protein 13WD+UTP13 TBL3 WD 4
UTP13
Q9NVX2|
NLE1_HUMA Notchless protein
14 N 724 homolog 1 8WD+NLE NLE1 WD
NLE 1
Q9UKB1|
FBW1B_HUM F-box/WD repeat-
15 AN 648 containing protein 11 7WD+FBOX FBXW11 WD
FBOX 1
Q9H2Y7|
ZF106_HUMA Zinc finger protein 106
16 N 687 homolog 6WD+1ZnF_C2H2 ZFP106 WD 0
ZnF_C2H2 0
tethering
middle c-termini functions number
transcription,transduction,regulation of transcription,DNA
dependent signal transduction,multicellular organismal
development,organ morphogenesis,wnt receptor signalling
pathway,negative regulation of transcription,negative
regulation of wnt receptor signalling pathway,regulation of
0 0 transcription 1 1GXR
0 6
0 0 1
transcription,transduction,regulation of transcription,DNA
dependent signal transduction,multicellular organismal
development,organ morphogenesis,wnt receptor signalling
pathway,negative regulation of transcription,negative
regulation of wnt receptor signalling pathway,regulation of
0 0 transcription 1 1GXR
regulation of transcription, DNA-dependent
biological_process,Wnt receptor signaling
0 0 pathway,regulation of transcription 1 1GXR
ubiquitin-dependent protein catabolic process,ubiquitin
cycle,multicellular organismal development,Wnt receptor
0 0 signaling pathway,embryonic limb morphogenesis 1
1 2
regulation of transcription, DNA-dependent,signal
transduction,multicellular organismal development,organ
0 0 morphogenesis,Wnt receptor signaling pathway 1 1GXR
1 5
7 regulation of transcription
7 regulation of transcription
ubiquitin cycle
7 regulation of transcription
7 regulation of transcription
7 regulation of transcription
7 regulation of transcription
regulation of transcription
cell communication
7 regulation of transcription
regulation of transcription
cell comunication
ubiquitin cycle
regulation of ranscription
pathway desease
it work in
Putative FAK1 pathway coplex(oligomerization)
it work in
Wnt receptor signaling pathway coplex(oligomerization)