Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 7 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 9 |
GO:0005885 | Arp2/3 protein complex | 2 | 9 |
GO:0032991 | protein-containing complex | 1 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4H3F1
Term | Name | Level | Count |
---|---|---|---|
GO:0007015 | actin filament organization | 5 | 9 |
GO:0008064 | regulation of actin polymerization or depolymerization | 6 | 9 |
GO:0008154 | actin polymerization or depolymerization | 6 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016043 | cellular component organization | 3 | 9 |
GO:0022607 | cellular component assembly | 4 | 9 |
GO:0030041 | actin filament polymerization | 7 | 9 |
GO:0030832 | regulation of actin filament length | 5 | 9 |
GO:0030833 | regulation of actin filament polymerization | 7 | 9 |
GO:0032271 | regulation of protein polymerization | 6 | 9 |
GO:0032535 | regulation of cellular component size | 4 | 9 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 9 |
GO:0032970 | regulation of actin filament-based process | 4 | 9 |
GO:0033043 | regulation of organelle organization | 5 | 9 |
GO:0034314 | Arp2/3 complex-mediated actin nucleation | 7 | 9 |
GO:0043254 | regulation of protein-containing complex assembly | 5 | 9 |
GO:0043933 | protein-containing complex organization | 4 | 9 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 9 |
GO:0045010 | actin nucleation | 6 | 9 |
GO:0050789 | regulation of biological process | 2 | 9 |
GO:0050794 | regulation of cellular process | 3 | 9 |
GO:0051128 | regulation of cellular component organization | 4 | 9 |
GO:0051258 | protein polymerization | 6 | 9 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 9 |
GO:0065003 | protein-containing complex assembly | 5 | 9 |
GO:0065007 | biological regulation | 1 | 9 |
GO:0065008 | regulation of biological quality | 2 | 9 |
GO:0071840 | cellular component organization or biogenesis | 2 | 9 |
GO:0090066 | regulation of anatomical structure size | 3 | 9 |
GO:0097435 | supramolecular fiber organization | 4 | 9 |
GO:0110053 | regulation of actin filament organization | 6 | 9 |
GO:1902903 | regulation of supramolecular fiber organization | 5 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0005515 | protein binding | 2 | 3 |
GO:0008092 | cytoskeletal protein binding | 3 | 3 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0051015 | actin filament binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.538 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.171 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.330 |
DEG_APCC_DBOX_1 | 13 | 21 | PF00400 | 0.484 |
DEG_COP1_1 | 27 | 38 | PF00400 | 0.440 |
DOC_CYCLIN_yCln2_LP_2 | 40 | 46 | PF00134 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 55 | 61 | PF00134 | 0.346 |
DOC_MAPK_MEF2A_6 | 14 | 22 | PF00069 | 0.432 |
DOC_PP1_RVXF_1 | 88 | 94 | PF00149 | 0.416 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.602 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.393 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.445 |
LIG_14-3-3_CanoR_1 | 169 | 173 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 174 | 180 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 90 | 94 | PF00244 | 0.429 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.432 |
LIG_BIR_III_2 | 48 | 52 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.422 |
LIG_eIF4E_1 | 153 | 159 | PF01652 | 0.429 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.496 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.496 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.522 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.391 |
LIG_LIR_Apic_2 | 204 | 209 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 111 | 117 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 204 | 208 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.371 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.410 |
LIG_SH2_NCK_1 | 9 | 13 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.371 |
LIG_SUMO_SIM_anti_2 | 37 | 42 | PF11976 | 0.470 |
LIG_TRAF2_2 | 209 | 214 | PF00917 | 0.402 |
LIG_TYR_ITIM | 7 | 12 | PF00017 | 0.410 |
LIG_WRC_WIRS_1 | 176 | 181 | PF05994 | 0.410 |
LIG_WRC_WIRS_1 | 22 | 27 | PF05994 | 0.484 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.407 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.435 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.485 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.474 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.371 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.454 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.460 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.201 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.284 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.400 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.549 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.493 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.444 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.171 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.180 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.518 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.416 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.400 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.485 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.431 |
MOD_NEK2_2 | 201 | 206 | PF00069 | 0.378 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.432 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.402 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.429 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.496 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.429 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.401 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.397 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.460 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.484 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.440 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.371 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.485 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.448 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.445 |
TRG_DiLeu_BaEn_1 | 13 | 18 | PF01217 | 0.432 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAU0 | Leptomonas seymouri | 45% | 100% |
A0A0S4KGM1 | Bodo saltans | 27% | 100% |
A0A1X0NJU3 | Trypanosomatidae | 29% | 100% |
A0A3R7MB12 | Trypanosoma rangeli | 26% | 100% |
A0A451EJJ5 | Leishmania donovani | 72% | 100% |
A4HRQ5 | Leishmania infantum | 71% | 100% |
C9ZJ46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AJM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
F4JUL9 | Arabidopsis thaliana | 28% | 100% |
O96625 | Dictyostelium discoideum | 25% | 100% |
P58798 | Caenorhabditis elegans | 28% | 100% |
P59998 | Homo sapiens | 28% | 100% |
P59999 | Mus musculus | 28% | 100% |
Q148J6 | Bos taurus | 28% | 100% |
Q19R45 | Leishmania major | 67% | 100% |
Q641G7 | Xenopus laevis | 28% | 100% |
Q92352 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |