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: 5 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 5, no: 6 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0005793 | endoplasmic reticulum-Golgi intermediate compartment | 5 | 1 |
GO:0030134 | COPII-coated ER to Golgi transport vesicle | 8 | 1 |
GO:0030135 | coated vesicle | 7 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: E8NHN5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007029 | endoplasmic reticulum organization | 5 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005537 | mannose binding | 4 | 1 |
GO:0030246 | carbohydrate binding | 2 | 2 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0048029 | monosaccharide binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.389 |
CLV_PCSK_FUR_1 | 535 | 539 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 592 | 594 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 536 | 538 | PF00082 | 0.710 |
CLV_PCSK_PC7_1 | 312 | 318 | PF00082 | 0.669 |
CLV_PCSK_PC7_1 | 324 | 330 | PF00082 | 0.608 |
CLV_PCSK_PC7_1 | 412 | 418 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.665 |
CLV_Separin_Metazoa | 497 | 501 | PF03568 | 0.466 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.557 |
DEG_APCC_DBOX_1 | 536 | 544 | PF00400 | 0.545 |
DEG_APCC_DBOX_1 | 561 | 569 | PF00400 | 0.348 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.556 |
DOC_CYCLIN_RxL_1 | 318 | 331 | PF00134 | 0.503 |
DOC_MAPK_gen_1 | 30 | 39 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 338 | 347 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 462 | 472 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 549 | 557 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 592 | 598 | PF00069 | 0.497 |
DOC_MAPK_HePTP_8 | 27 | 39 | PF00069 | 0.545 |
DOC_MAPK_JIP1_4 | 33 | 39 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 30 | 39 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 338 | 347 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 465 | 472 | PF00069 | 0.318 |
DOC_PP1_RVXF_1 | 593 | 599 | PF00149 | 0.515 |
DOC_PP2B_LxvP_1 | 37 | 40 | PF13499 | 0.547 |
DOC_PP2B_LxvP_1 | 391 | 394 | PF13499 | 0.377 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.270 |
DOC_SPAK_OSR1_1 | 212 | 216 | PF12202 | 0.270 |
DOC_SPAK_OSR1_1 | 42 | 46 | PF12202 | 0.186 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.514 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.431 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 184 | 190 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 2 | 12 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 329 | 334 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 538 | 544 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 84 | 90 | PF00244 | 0.620 |
LIG_deltaCOP1_diTrp_1 | 205 | 213 | PF00928 | 0.357 |
LIG_deltaCOP1_diTrp_1 | 272 | 280 | PF00928 | 0.489 |
LIG_eIF4E_1 | 53 | 59 | PF01652 | 0.186 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.303 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.308 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.417 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.364 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.448 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.505 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.358 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.541 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.450 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.373 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.407 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.405 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.553 |
LIG_LIR_Apic_2 | 151 | 157 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 180 | 190 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 385 | 394 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 551 | 560 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 551 | 555 | PF02991 | 0.450 |
LIG_NRBOX | 67 | 73 | PF00104 | 0.186 |
LIG_PDZ_Class_3 | 606 | 611 | PF00595 | 0.573 |
LIG_Pex14_2 | 323 | 327 | PF04695 | 0.503 |
LIG_Pex14_2 | 350 | 354 | PF04695 | 0.366 |
LIG_PTB_Apo_2 | 176 | 183 | PF02174 | 0.284 |
LIG_REV1ctd_RIR_1 | 78 | 88 | PF16727 | 0.560 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 502 | 506 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 577 | 581 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 241 | 244 | PF00017 | 0.284 |
LIG_SH2_STAT3 | 463 | 466 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.455 |
LIG_SH3_1 | 600 | 606 | PF00018 | 0.471 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.553 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.497 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.471 |
LIG_SUMO_SIM_anti_2 | 454 | 461 | PF11976 | 0.318 |
LIG_SUMO_SIM_anti_2 | 493 | 501 | PF11976 | 0.469 |
LIG_SUMO_SIM_anti_2 | 55 | 60 | PF11976 | 0.177 |
LIG_SUMO_SIM_anti_2 | 64 | 70 | PF11976 | 0.172 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.401 |
LIG_TRAF2_1 | 298 | 301 | PF00917 | 0.535 |
LIG_TRAF2_1 | 452 | 455 | PF00917 | 0.404 |
LIG_UBA3_1 | 322 | 328 | PF00899 | 0.642 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.428 |
MOD_CDK_SPxxK_3 | 258 | 265 | PF00069 | 0.673 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.439 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.665 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.437 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.560 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.527 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.443 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.679 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.538 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.528 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.511 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.433 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.318 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.422 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.672 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.399 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.674 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.545 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.683 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.611 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.617 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.457 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.496 |
MOD_LATS_1 | 82 | 88 | PF00433 | 0.443 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.425 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.650 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.442 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.420 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.438 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.403 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.379 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.403 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.510 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.671 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.583 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.515 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.217 |
MOD_NEK2_2 | 539 | 544 | PF00069 | 0.660 |
MOD_PK_1 | 329 | 335 | PF00069 | 0.593 |
MOD_PKA_1 | 311 | 317 | PF00069 | 0.660 |
MOD_PKA_1 | 328 | 334 | PF00069 | 0.496 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.286 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.336 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.321 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.641 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.445 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.516 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.663 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.337 |
MOD_Plk_1 | 480 | 486 | PF00069 | 0.554 |
MOD_Plk_2-3 | 295 | 301 | PF00069 | 0.686 |
MOD_Plk_2-3 | 481 | 487 | PF00069 | 0.522 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.383 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.622 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.496 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.572 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.396 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.497 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.207 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.175 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.480 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.674 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.426 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.543 |
MOD_SUMO_for_1 | 478 | 481 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 542 | 552 | PF00179 | 0.635 |
MOD_SUMO_rev_2 | 567 | 575 | PF00179 | 0.438 |
TRG_DiLeu_BaEn_1 | 455 | 460 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_2 | 14 | 20 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 144 | 149 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 535 | 538 | PF00400 | 0.661 |
TRG_NES_CRM1_1 | 559 | 571 | PF08389 | 0.552 |
TRG_NLS_MonoCore_2 | 314 | 319 | PF00514 | 0.632 |
TRG_NLS_MonoCore_2 | 534 | 539 | PF00514 | 0.655 |
TRG_NLS_MonoExtC_3 | 314 | 319 | PF00514 | 0.632 |
TRG_NLS_MonoExtC_3 | 534 | 539 | PF00514 | 0.655 |
TRG_NLS_MonoExtN_4 | 312 | 319 | PF00514 | 0.645 |
TRG_NLS_MonoExtN_4 | 533 | 540 | PF00514 | 0.660 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIA0 | Leptomonas seymouri | 77% | 100% |
A0A1X0NKB0 | Trypanosomatidae | 43% | 94% |
A0A3R7LT82 | Trypanosoma rangeli | 47% | 100% |
A0A3S5H5L7 | Leishmania donovani | 88% | 100% |
A4H4F2 | Leishmania braziliensis | 88% | 100% |
A4HSM9 | Leishmania infantum | 93% | 100% |
C9ZU67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 98% |
E9AKL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 100% | 100% |
Q4QJ95 | Leishmania major | 94% | 100% |
V5ARI9 | Trypanosoma cruzi | 47% | 100% |