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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4Q4D4
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 9 |
GO:0022857 | transmembrane transporter activity | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.628 |
CLV_C14_Caspase3-7 | 166 | 170 | PF00656 | 0.685 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.431 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.243 |
DEG_APCC_DBOX_1 | 147 | 155 | PF00400 | 0.558 |
DEG_MDM2_SWIB_1 | 472 | 480 | PF02201 | 0.311 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.612 |
DEG_SPOP_SBC_1 | 393 | 397 | PF00917 | 0.431 |
DOC_AGCK_PIF_1 | 30 | 35 | PF00069 | 0.358 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.268 |
DOC_CYCLIN_yCln2_LP_2 | 543 | 549 | PF00134 | 0.266 |
DOC_CYCLIN_yCln2_LP_2 | 57 | 63 | PF00134 | 0.223 |
DOC_MAPK_gen_1 | 421 | 431 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 572 | 580 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 72 | 80 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 424 | 431 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 72 | 80 | PF00069 | 0.474 |
DOC_MAPK_NFAT4_5 | 424 | 432 | PF00069 | 0.298 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.259 |
DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.259 |
DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.566 |
DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.266 |
DOC_PP4_FxxP_1 | 255 | 258 | PF00568 | 0.298 |
DOC_PP4_FxxP_1 | 556 | 559 | PF00568 | 0.347 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.395 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.248 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 181 | 187 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 317 | 321 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 417 | 421 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 536 | 545 | PF00244 | 0.231 |
LIG_14-3-3_CanoR_1 | 77 | 86 | PF00244 | 0.443 |
LIG_Actin_WH2_2 | 25 | 43 | PF00022 | 0.250 |
LIG_Actin_WH2_2 | 316 | 333 | PF00022 | 0.530 |
LIG_BIR_III_4 | 405 | 409 | PF00653 | 0.492 |
LIG_BRCT_BRCA1_1 | 235 | 239 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 618 | 622 | PF00533 | 0.335 |
LIG_Clathr_ClatBox_1 | 14 | 18 | PF01394 | 0.465 |
LIG_eIF4E_1 | 279 | 285 | PF01652 | 0.259 |
LIG_eIF4E_1 | 86 | 92 | PF01652 | 0.342 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.475 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.633 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.450 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.433 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.346 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.454 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.485 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.354 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.302 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.362 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.637 |
LIG_FHA_2 | 558 | 564 | PF00498 | 0.437 |
LIG_LIR_Apic_2 | 477 | 482 | PF02991 | 0.494 |
LIG_LIR_Apic_2 | 554 | 559 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 312 | 321 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 34 | 40 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 352 | 361 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 459 | 469 | PF02991 | 0.236 |
LIG_LIR_Gen_1 | 539 | 549 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 9 | 20 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 312 | 316 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 34 | 38 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 619 | 625 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.500 |
LIG_Pex14_2 | 19 | 23 | PF04695 | 0.422 |
LIG_Pex14_2 | 472 | 476 | PF04695 | 0.406 |
LIG_Pex14_2 | 552 | 556 | PF04695 | 0.320 |
LIG_PTB_Apo_2 | 49 | 56 | PF02174 | 0.266 |
LIG_PTB_Phospho_1 | 49 | 55 | PF10480 | 0.266 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.350 |
LIG_SH2_CRK | 35 | 39 | PF00017 | 0.298 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.418 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 26 | 30 | PF00017 | 0.358 |
LIG_SH2_NCK_1 | 567 | 571 | PF00017 | 0.393 |
LIG_SH2_PTP2 | 55 | 58 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.619 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 281 | 285 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 86 | 90 | PF00017 | 0.294 |
LIG_SH2_STAT3 | 547 | 550 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.206 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.196 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.162 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.358 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.313 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.542 |
LIG_SUMO_SIM_anti_2 | 89 | 94 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 36 | 42 | PF11976 | 0.379 |
LIG_TRFH_1 | 55 | 59 | PF08558 | 0.266 |
LIG_TRFH_1 | 593 | 597 | PF08558 | 0.276 |
LIG_TYR_ITIM | 351 | 356 | PF00017 | 0.418 |
LIG_WRC_WIRS_1 | 280 | 285 | PF05994 | 0.347 |
LIG_WRC_WIRS_1 | 608 | 613 | PF05994 | 0.311 |
MOD_CDK_SPxxK_3 | 593 | 600 | PF00069 | 0.248 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.358 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.467 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.570 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.542 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.266 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.276 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.513 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.437 |
MOD_CMANNOS | 476 | 479 | PF00535 | 0.294 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.266 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.320 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.263 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.371 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.268 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.477 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.205 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.271 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.310 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.397 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.713 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.283 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.450 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.536 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.232 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.626 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.489 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.325 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.266 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.266 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.486 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.283 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.235 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.364 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.285 |
MOD_NEK2_2 | 127 | 132 | PF00069 | 0.358 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.633 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.393 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.502 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.501 |
MOD_PK_1 | 357 | 363 | PF00069 | 0.443 |
MOD_PKA_1 | 536 | 542 | PF00069 | 0.231 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.557 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.455 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.502 |
MOD_PKB_1 | 486 | 494 | PF00069 | 0.431 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.736 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.633 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.632 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.456 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.265 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.426 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.469 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.290 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.462 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.292 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.307 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.437 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.437 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.266 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.636 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.367 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.248 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.266 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.206 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.162 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C4 | Leptomonas seymouri | 58% | 96% |
A0A1X0P0R8 | Trypanosomatidae | 39% | 95% |
A0A3S7X6J4 | Leishmania donovani | 91% | 100% |
A4HLB1 | Leishmania braziliensis | 74% | 100% |
A4I8T7 | Leishmania infantum | 91% | 100% |
E9B3Q3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5BPE7 | Trypanosoma cruzi | 38% | 100% |