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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005885 | Arp2/3 protein complex | 2 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
Related structures:
AlphaFold database: A4HXW5
Term | Name | Level | Count |
---|---|---|---|
GO:0007015 | actin filament organization | 5 | 7 |
GO:0008064 | regulation of actin polymerization or depolymerization | 6 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0030832 | regulation of actin filament length | 5 | 7 |
GO:0030833 | regulation of actin filament polymerization | 7 | 7 |
GO:0032271 | regulation of protein polymerization | 6 | 7 |
GO:0032535 | regulation of cellular component size | 4 | 7 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 7 |
GO:0032970 | regulation of actin filament-based process | 4 | 7 |
GO:0033043 | regulation of organelle organization | 5 | 7 |
GO:0034314 | Arp2/3 complex-mediated actin nucleation | 7 | 7 |
GO:0043254 | regulation of protein-containing complex assembly | 5 | 7 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 7 |
GO:0045010 | actin nucleation | 6 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051128 | regulation of cellular component organization | 4 | 7 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065008 | regulation of biological quality | 2 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
GO:0090066 | regulation of anatomical structure size | 3 | 7 |
GO:0097435 | supramolecular fiber organization | 4 | 7 |
GO:0110053 | regulation of actin filament organization | 6 | 7 |
GO:1902903 | regulation of supramolecular fiber organization | 5 | 7 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0030029 | actin filament-based process | 2 | 1 |
GO:0030036 | actin cytoskeleton organization | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005515 | protein binding | 2 | 7 |
GO:0008092 | cytoskeletal protein binding | 3 | 7 |
GO:0005198 | structural molecule activity | 1 | 1 |
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 | 12 | 16 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.452 |
DEG_APCC_DBOX_1 | 601 | 609 | PF00400 | 0.459 |
DEG_SCF_TRCP1_1 | 336 | 341 | PF00400 | 0.401 |
DEG_SIAH_1 | 85 | 93 | PF03145 | 0.483 |
DEG_SPOP_SBC_1 | 347 | 351 | PF00917 | 0.558 |
DEG_SPOP_SBC_1 | 529 | 533 | PF00917 | 0.563 |
DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.605 |
DEG_SPOP_SBC_1 | 79 | 83 | PF00917 | 0.591 |
DOC_ANK_TNKS_1 | 535 | 542 | PF00023 | 0.603 |
DOC_CDC14_PxL_1 | 169 | 177 | PF14671 | 0.389 |
DOC_CDC14_PxL_1 | 379 | 387 | PF14671 | 0.462 |
DOC_MAPK_gen_1 | 506 | 515 | PF00069 | 0.547 |
DOC_MAPK_HePTP_8 | 503 | 515 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 506 | 515 | PF00069 | 0.547 |
DOC_PP4_FxxP_1 | 232 | 235 | PF00568 | 0.505 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 562 | 567 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 228 | 233 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 246 | 251 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 471 | 479 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 534 | 540 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 559 | 567 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 609 | 614 | PF00244 | 0.507 |
LIG_CSL_BTD_1 | 133 | 136 | PF09270 | 0.447 |
LIG_CSL_BTD_1 | 322 | 325 | PF09270 | 0.440 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.475 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.433 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.580 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.364 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.487 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.790 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.556 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.441 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.555 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.636 |
LIG_LIR_Apic_2 | 230 | 235 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 166 | 177 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.479 |
LIG_MYND_1 | 21 | 25 | PF01753 | 0.634 |
LIG_NRBOX | 570 | 576 | PF00104 | 0.359 |
LIG_REV1ctd_RIR_1 | 513 | 522 | PF16727 | 0.553 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.370 |
LIG_SH3_1 | 22 | 28 | PF00018 | 0.519 |
LIG_SH3_1 | 617 | 623 | PF00018 | 0.677 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.446 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.541 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.599 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.432 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.675 |
LIG_SUMO_SIM_anti_2 | 569 | 576 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 174 | 181 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 478 | 483 | PF11976 | 0.574 |
LIG_UBA3_1 | 574 | 583 | PF00899 | 0.538 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.556 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.441 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.624 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.603 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.584 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.623 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.721 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.511 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.388 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.619 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.642 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.387 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.324 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.651 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.639 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.558 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.429 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.494 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.653 |
MOD_GlcNHglycan | 360 | 365 | PF01048 | 0.675 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.547 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.551 |
MOD_GlcNHglycan | 437 | 441 | PF01048 | 0.763 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.555 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.488 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.597 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.385 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.440 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.643 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.457 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.505 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.408 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.475 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.682 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.529 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.692 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.599 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.690 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.652 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.666 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.582 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.617 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.507 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.571 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.551 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.450 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.477 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.312 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.682 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.584 |
MOD_PIKK_1 | 492 | 498 | PF00454 | 0.657 |
MOD_PK_1 | 246 | 252 | PF00069 | 0.469 |
MOD_PKA_1 | 228 | 234 | PF00069 | 0.538 |
MOD_PKA_1 | 444 | 450 | PF00069 | 0.622 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.528 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.689 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.657 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.749 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.617 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.671 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.494 |
MOD_PKB_1 | 607 | 615 | PF00069 | 0.493 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.407 |
MOD_Plk_2-3 | 388 | 394 | PF00069 | 0.443 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.538 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.437 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.426 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.399 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.595 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.367 |
MOD_ProDKin_1 | 562 | 568 | PF00069 | 0.574 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.585 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 219 | 224 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 380 | 385 | PF01217 | 0.470 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 606 | 609 | PF00400 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8H8 | Leptomonas seymouri | 38% | 100% |
A0A3Q8IA03 | Leishmania donovani | 100% | 100% |
A4H9K0 | Leishmania braziliensis | 60% | 89% |
E9ARM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 99% |
Q4QDV0 | Leishmania major | 89% | 100% |