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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 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 |
Related structures:
AlphaFold database: A0A3Q8IH23
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.448 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 200 | 202 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 559 | 561 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.407 |
DEG_APCC_DBOX_1 | 342 | 350 | PF00400 | 0.480 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.447 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.551 |
DEG_MDM2_SWIB_1 | 118 | 125 | PF02201 | 0.420 |
DEG_SPOP_SBC_1 | 384 | 388 | PF00917 | 0.210 |
DOC_CDC14_PxL_1 | 303 | 311 | PF14671 | 0.387 |
DOC_CYCLIN_RxL_1 | 399 | 407 | PF00134 | 0.466 |
DOC_CYCLIN_RxL_1 | 4 | 14 | PF00134 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 125 | 131 | PF00134 | 0.324 |
DOC_CYCLIN_yCln2_LP_2 | 471 | 477 | PF00134 | 0.409 |
DOC_MAPK_gen_1 | 273 | 282 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 341 | 350 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 558 | 568 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 59 | 67 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 6 | 12 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 341 | 349 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 367 | 374 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 453 | 462 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 548 | 555 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 61 | 69 | PF00069 | 0.338 |
DOC_MAPK_NFAT4_5 | 341 | 349 | PF00069 | 0.520 |
DOC_PP1_RVXF_1 | 546 | 553 | PF00149 | 0.611 |
DOC_PP2B_LxvP_1 | 125 | 128 | PF13499 | 0.348 |
DOC_PP2B_LxvP_1 | 471 | 474 | PF13499 | 0.496 |
DOC_PP4_FxxP_1 | 327 | 330 | PF00568 | 0.392 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.412 |
DOC_USP7_MATH_2 | 447 | 453 | PF00917 | 0.516 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 229 | 238 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 268 | 272 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 438 | 444 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 453 | 458 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 500 | 508 | PF00244 | 0.394 |
LIG_Actin_WH2_2 | 48 | 63 | PF00022 | 0.412 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.648 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.233 |
LIG_BRCT_BRCA1_1 | 503 | 507 | PF00533 | 0.441 |
LIG_CaM_IQ_9 | 260 | 276 | PF13499 | 0.537 |
LIG_CaM_IQ_9 | 550 | 566 | PF13499 | 0.622 |
LIG_Clathr_ClatBox_1 | 39 | 43 | PF01394 | 0.392 |
LIG_eIF4E_1 | 34 | 40 | PF01652 | 0.372 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.429 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.483 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.399 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.424 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.293 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.694 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.605 |
LIG_LIR_Apic_2 | 326 | 330 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 121 | 125 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 262 | 266 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.390 |
LIG_NRBOX | 345 | 351 | PF00104 | 0.423 |
LIG_NRBOX | 396 | 402 | PF00104 | 0.406 |
LIG_Pex14_1 | 539 | 543 | PF04695 | 0.493 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.306 |
LIG_Pex14_2 | 203 | 207 | PF04695 | 0.340 |
LIG_Pex14_2 | 26 | 30 | PF04695 | 0.420 |
LIG_Pex14_2 | 462 | 466 | PF04695 | 0.454 |
LIG_Pex14_2 | 503 | 507 | PF04695 | 0.371 |
LIG_REV1ctd_RIR_1 | 362 | 371 | PF16727 | 0.450 |
LIG_SH2_GRB2like | 542 | 545 | PF00017 | 0.586 |
LIG_SH2_SRC | 288 | 291 | PF00017 | 0.388 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 288 | 292 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.328 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.433 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.472 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.580 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.626 |
LIG_SUMO_SIM_anti_2 | 456 | 461 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 517 | 525 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 517 | 525 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 8 | 14 | PF11976 | 0.576 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.691 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.658 |
LIG_UBA3_1 | 551 | 559 | PF00899 | 0.435 |
MOD_CDC14_SPxK_1 | 198 | 201 | PF00782 | 0.497 |
MOD_CDK_SPK_2 | 195 | 200 | PF00069 | 0.467 |
MOD_CDK_SPK_2 | 99 | 104 | PF00069 | 0.521 |
MOD_CDK_SPxK_1 | 195 | 201 | PF00069 | 0.474 |
MOD_CDK_SPxxK_3 | 195 | 202 | PF00069 | 0.423 |
MOD_CDK_SPxxK_3 | 99 | 106 | PF00069 | 0.518 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.396 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.687 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.645 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.650 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.443 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.596 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.666 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.388 |
MOD_Cter_Amidation | 339 | 342 | PF01082 | 0.353 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.596 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.370 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.391 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.399 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.386 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.603 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.434 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.471 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.571 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.416 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.670 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.593 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.476 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.545 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.609 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.669 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.430 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.397 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.635 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.515 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.505 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.659 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.403 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.476 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.358 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.428 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.396 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.330 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.545 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.222 |
MOD_NEK2_2 | 522 | 527 | PF00069 | 0.388 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.589 |
MOD_PIKK_1 | 480 | 486 | PF00454 | 0.539 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.358 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.410 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.502 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.482 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.519 |
MOD_PKB_1 | 104 | 112 | PF00069 | 0.470 |
MOD_PKB_1 | 227 | 235 | PF00069 | 0.514 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.702 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.373 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.665 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.317 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.306 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.610 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.443 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.300 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.433 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.340 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.522 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.321 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.334 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.392 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.470 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.474 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.519 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.583 |
MOD_SUMO_for_1 | 166 | 169 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_1 | 546 | 551 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_2 | 261 | 267 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 399 | 404 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 438 | 440 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.517 |
TRG_NES_CRM1_1 | 20 | 32 | PF08389 | 0.402 |
TRG_NLS_MonoExtN_4 | 199 | 204 | PF00514 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 402 | 406 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVM9 | Leptomonas seymouri | 44% | 100% |
A0A1X0NZT8 | Trypanosomatidae | 24% | 100% |
A0A3R7KT94 | Trypanosoma rangeli | 26% | 100% |
A4HH24 | Leishmania braziliensis | 73% | 100% |
A4I453 | Leishmania infantum | 100% | 100% |
C9ZKQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9ADL8 | Leishmania major | 90% | 100% |
E9AM63 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B4T3 | Trypanosoma cruzi | 25% | 100% |