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: E9ARM9
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 | 0.587 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 600 | 608 | PF00400 | 0.461 |
DEG_SCF_TRCP1_1 | 339 | 344 | PF00400 | 0.399 |
DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.501 |
DEG_SPOP_SBC_1 | 350 | 354 | PF00917 | 0.526 |
DEG_SPOP_SBC_1 | 545 | 549 | PF00917 | 0.608 |
DOC_ANK_TNKS_1 | 538 | 545 | PF00023 | 0.603 |
DOC_CDC14_PxL_1 | 172 | 180 | PF14671 | 0.386 |
DOC_CDC14_PxL_1 | 382 | 390 | PF14671 | 0.453 |
DOC_MAPK_gen_1 | 509 | 518 | PF00069 | 0.518 |
DOC_MAPK_HePTP_8 | 506 | 518 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 509 | 518 | PF00069 | 0.518 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.763 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.596 |
LIG_14-3-3_CanoR_1 | 231 | 235 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 351 | 356 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 423 | 428 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 474 | 482 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 564 | 570 | PF00244 | 0.583 |
LIG_CSL_BTD_1 | 134 | 137 | PF09270 | 0.455 |
LIG_CSL_BTD_1 | 325 | 328 | PF09270 | 0.439 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.489 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.445 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.604 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.363 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.479 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.795 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.636 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.448 |
LIG_LIR_Apic_2 | 81 | 87 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 169 | 180 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.457 |
LIG_MYND_1 | 21 | 25 | PF01753 | 0.652 |
LIG_REV1ctd_RIR_1 | 516 | 525 | PF16727 | 0.512 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.377 |
LIG_SH3_1 | 232 | 238 | PF00018 | 0.469 |
LIG_SH3_1 | 616 | 622 | PF00018 | 0.686 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.453 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.469 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.557 |
LIG_SH3_3 | 616 | 622 | PF00018 | 0.684 |
LIG_SUMO_SIM_anti_2 | 568 | 575 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 177 | 182 | PF11976 | 0.353 |
LIG_UBA3_1 | 573 | 582 | PF00899 | 0.557 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.560 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.452 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.498 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.452 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.644 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.601 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.527 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.723 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.463 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.396 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.641 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.556 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.362 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.388 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.338 |
MOD_GlcNHglycan | 237 | 241 | PF01048 | 0.547 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.543 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.638 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.558 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.425 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.494 |
MOD_GlcNHglycan | 364 | 368 | PF01048 | 0.642 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.437 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.538 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.763 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.609 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.706 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.568 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.597 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.504 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.594 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.390 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.451 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.463 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.497 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.405 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.659 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.490 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.511 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.683 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.616 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.680 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.679 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.438 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.531 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.607 |
MOD_N-GLC_1 | 589 | 594 | PF02516 | 0.342 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.513 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.569 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.514 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.597 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.497 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.664 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.572 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.656 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.548 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.657 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.623 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.610 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.620 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.409 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.508 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.536 |
MOD_Plk_1 | 589 | 595 | PF00069 | 0.435 |
MOD_Plk_2-3 | 391 | 397 | PF00069 | 0.442 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.509 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.427 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.476 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.471 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.406 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.367 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.513 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.602 |
TRG_DiLeu_BaLyEn_6 | 222 | 227 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 383 | 388 | PF01217 | 0.459 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 493 | 497 | PF00026 | 0.527 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8H8 | Leptomonas seymouri | 37% | 100% |
A0A3Q8IA03 | Leishmania donovani | 85% | 100% |
A4H9K0 | Leishmania braziliensis | 70% | 100% |
A4HXW5 | Leishmania infantum | 85% | 100% |
Q4QDV0 | Leishmania major | 84% | 100% |