Structural Proteins, actin-like
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: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005884 | actin filament | 6 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
Related structures:
AlphaFold database: A0A3Q8I9L1
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 1 |
GO:0005200 | structural constituent of cytoskeleton | 2 | 1 |
GO:0098918 | structural constituent of synapse | 2 | 1 |
GO:0098973 | structural constituent of postsynaptic actin cytoskeleton | 3 | 1 |
GO:0099186 | structural constituent of postsynapse | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.340 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.217 |
DEG_MDM2_SWIB_1 | 77 | 84 | PF02201 | 0.540 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.657 |
DEG_SCF_TRCP1_1 | 156 | 162 | PF00400 | 0.469 |
DOC_CKS1_1 | 235 | 240 | PF01111 | 0.540 |
DOC_CYCLIN_yCln2_LP_2 | 107 | 113 | PF00134 | 0.417 |
DOC_MAPK_MEF2A_6 | 118 | 126 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 372 | 379 | PF00149 | 0.537 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.487 |
DOC_PP4_FxxP_1 | 314 | 317 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.540 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 175 | 182 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 256 | 265 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 300 | 308 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 321 | 329 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 443 | 449 | PF00244 | 0.543 |
LIG_Actin_WH2_2 | 84 | 99 | PF00022 | 0.510 |
LIG_BRCT_BRCA1_1 | 404 | 408 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 80 | 88 | PF00928 | 0.497 |
LIG_eIF4E_1 | 338 | 344 | PF01652 | 0.570 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.508 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.417 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.469 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.463 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.462 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.487 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.515 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.370 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.471 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.422 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.469 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 217 | 223 | PF02991 | 0.536 |
LIG_LIR_Apic_2 | 311 | 317 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 169 | 177 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 457 | 465 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 80 | 87 | PF02991 | 0.471 |
LIG_LIR_LC3C_4 | 150 | 155 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 377 | 381 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 457 | 463 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.455 |
LIG_NRBOX | 190 | 196 | PF00104 | 0.487 |
LIG_PCNA_PIPBox_1 | 456 | 465 | PF02747 | 0.540 |
LIG_Pex14_1 | 88 | 92 | PF04695 | 0.530 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.455 |
LIG_Pex14_2 | 77 | 81 | PF04695 | 0.540 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.581 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.570 |
LIG_SH2_GRB2like | 396 | 399 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 236 | 240 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 329 | 333 | PF00017 | 0.542 |
LIG_SH2_PTP2 | 220 | 223 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.542 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 445 | 449 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.453 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.476 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.487 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 121 | 128 | PF11976 | 0.469 |
LIG_SUMO_SIM_anti_2 | 339 | 346 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 138 | 146 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 339 | 346 | PF11976 | 0.523 |
LIG_TRAF2_1 | 206 | 209 | PF00917 | 0.560 |
LIG_TRAF2_2 | 434 | 439 | PF00917 | 0.542 |
LIG_TYR_ITIM | 478 | 483 | PF00017 | 0.540 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.469 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.510 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.536 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.515 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.567 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.469 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.540 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.525 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.469 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.431 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.555 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.569 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.532 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.469 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.531 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.269 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.223 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.240 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.296 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.336 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.274 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.352 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.354 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.469 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.493 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.538 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.403 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.451 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.597 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.340 |
MOD_N-GLC_2 | 385 | 387 | PF02516 | 0.269 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.570 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.334 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.469 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.503 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.544 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.355 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.510 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.510 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.473 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.458 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.556 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.469 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.512 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.515 |
MOD_PK_1 | 41 | 47 | PF00069 | 0.570 |
MOD_PKA_1 | 256 | 262 | PF00069 | 0.570 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.567 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.577 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.469 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.469 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.510 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.510 |
MOD_Plk_2-3 | 350 | 356 | PF00069 | 0.515 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.469 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.469 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.487 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.540 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.570 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.483 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.570 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.515 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.541 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.481 |
TRG_DiLeu_BaEn_1 | 169 | 174 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_2 | 100 | 106 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.602 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 420 | 425 | PF00026 | 0.340 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P696 | Leptomonas seymouri | 27% | 100% |
A0A0N0P8M2 | Leptomonas seymouri | 72% | 100% |
A0A0N1I659 | Leptomonas seymouri | 26% | 97% |
A0A0N1IM09 | Leptomonas seymouri | 24% | 100% |
A0A1X0NJ12 | Trypanosomatidae | 23% | 100% |
A0A3Q8IEK0 | Leishmania donovani | 24% | 100% |
A0A3Q8IJ53 | Leishmania donovani | 26% | 93% |
A0A422NGD7 | Trypanosoma rangeli | 53% | 100% |
A0A422NI92 | Trypanosoma rangeli | 26% | 100% |
A0A422NRB8 | Trypanosoma rangeli | 26% | 100% |
A2WNB0 | Oryza sativa subsp. indica | 26% | 100% |
A4FUX8 | Bos taurus | 24% | 100% |
A4H783 | Leishmania braziliensis | 83% | 100% |
A4HA61 | Leishmania braziliensis | 24% | 85% |
A4HMB0 | Leishmania braziliensis | 25% | 92% |
A4HVM3 | Leishmania infantum | 100% | 100% |
A4HYD8 | Leishmania infantum | 23% | 89% |
A4IAX6 | Leishmania infantum | 26% | 93% |
C9ZXR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A6N1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9APB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9AQC5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 91% |
E9AS71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B5V9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 93% |
O94805 | Homo sapiens | 24% | 100% |
O96019 | Homo sapiens | 25% | 100% |
P02581 | Glycine max | 30% | 100% |
P86173 | Rattus norvegicus | 24% | 100% |
Q09443 | Caenorhabditis elegans | 21% | 100% |
Q09849 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q4FX37 | Leishmania major | 26% | 93% |
Q4P2E8 | Ustilago maydis (strain 521 / FGSC 9021) | 24% | 90% |
Q4QD95 | Leishmania major | 25% | 89% |
Q4QG59 | Leishmania major | 97% | 100% |
Q4R333 | Macaca fascicularis | 25% | 100% |
Q4W9M3 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 24% | 100% |
Q4WHA3 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 25% | 100% |
Q54HF0 | Dictyostelium discoideum | 30% | 100% |
Q54KZ7 | Dictyostelium discoideum | 22% | 99% |
Q5AXH1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 22% | 100% |
Q5NBI2 | Oryza sativa subsp. japonica | 26% | 100% |
Q6BXN0 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 23% | 98% |
Q6C061 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 24% | 100% |
Q7S6X6 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 25% | 100% |
Q84M92 | Arabidopsis thaliana | 27% | 100% |
Q8LGE3 | Arabidopsis thaliana | 29% | 100% |
Q8RYC2 | Arabidopsis thaliana | 32% | 100% |
Q99MR0 | Mus musculus | 24% | 100% |
Q9D864 | Mus musculus | 22% | 100% |
Q9DEE9 | Gallus gallus | 23% | 100% |
Q9GZN1 | Homo sapiens | 21% | 100% |
Q9P7X7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q9Z2N8 | Mus musculus | 24% | 100% |
V5AVP6 | Trypanosoma cruzi | 50% | 100% |
V5DJL3 | Trypanosoma cruzi | 27% | 100% |