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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HAK0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 471 | 475 | PF00656 | 0.581 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.557 |
CLV_PCSK_FUR_1 | 385 | 389 | PF00082 | 0.479 |
CLV_PCSK_FUR_1 | 76 | 80 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 446 | 448 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 534 | 536 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.354 |
CLV_PCSK_PC7_1 | 421 | 427 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.612 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 172 | 178 | PF00134 | 0.606 |
DOC_MAPK_JIP1_4 | 61 | 67 | PF00069 | 0.402 |
DOC_PP1_RVXF_1 | 98 | 104 | PF00149 | 0.406 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.492 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.527 |
DOC_USP7_UBL2_3 | 424 | 428 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 9 | 18 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 517 | 533 | PF00022 | 0.585 |
LIG_deltaCOP1_diTrp_1 | 395 | 399 | PF00928 | 0.642 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.418 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.513 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.483 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.521 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.643 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.491 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.613 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.647 |
LIG_LIR_Apic_2 | 15 | 21 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 353 | 358 | PF02991 | 0.577 |
LIG_LIR_Apic_2 | 4 | 10 | PF02991 | 0.575 |
LIG_LIR_Apic_2 | 92 | 98 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 155 | 159 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.493 |
LIG_PCNA_yPIPBox_3 | 401 | 415 | PF02747 | 0.541 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.553 |
LIG_SH2_NCK_1 | 18 | 22 | PF00017 | 0.594 |
LIG_SH2_NCK_1 | 355 | 359 | PF00017 | 0.578 |
LIG_SH2_SRC | 411 | 414 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 311 | 314 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.536 |
LIG_SH3_1 | 417 | 423 | PF00018 | 0.573 |
LIG_SH3_2 | 420 | 425 | PF14604 | 0.567 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.573 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.637 |
LIG_TRAF2_1 | 441 | 444 | PF00917 | 0.609 |
LIG_TRAF2_1 | 458 | 461 | PF00917 | 0.753 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.657 |
LIG_UBA3_1 | 153 | 160 | PF00899 | 0.478 |
LIG_UBA3_1 | 523 | 531 | PF00899 | 0.574 |
LIG_WW_3 | 363 | 367 | PF00397 | 0.528 |
MOD_CDK_SPxK_1 | 140 | 146 | PF00069 | 0.577 |
MOD_CDK_SPxK_1 | 534 | 540 | PF00069 | 0.526 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.467 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.518 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.556 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.765 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.491 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.604 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.521 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.537 |
MOD_CMANNOS | 380 | 383 | PF00535 | 0.413 |
MOD_CMANNOS | 396 | 399 | PF00535 | 0.501 |
MOD_Cter_Amidation | 444 | 447 | PF01082 | 0.529 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.607 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.554 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.502 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.550 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.537 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.668 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.591 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.486 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.325 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.513 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.571 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.578 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.522 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.435 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.265 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.455 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.524 |
MOD_OFUCOSY | 256 | 262 | PF10250 | 0.432 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.436 |
MOD_PKA_1 | 424 | 430 | PF00069 | 0.522 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.531 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.512 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.580 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.566 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.414 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.536 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.470 |
MOD_Plk_2-3 | 438 | 444 | PF00069 | 0.642 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.472 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.595 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.532 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.578 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.590 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.638 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.479 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.531 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.526 |
MOD_SUMO_rev_2 | 432 | 442 | PF00179 | 0.685 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.535 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 333 | 336 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 384 | 387 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.548 |
TRG_NLS_Bipartite_1 | 415 | 429 | PF00514 | 0.536 |
TRG_NLS_MonoExtC_3 | 423 | 428 | PF00514 | 0.586 |
TRG_NLS_MonoExtN_4 | 421 | 428 | PF00514 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2A7 | Leptomonas seymouri | 53% | 100% |
A0A3S7X7L7 | Leishmania donovani | 75% | 98% |
A4I9P4 | Leishmania infantum | 74% | 98% |
E9B4Q8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 96% |
Q4Q3B8 | Leishmania major | 76% | 100% |
V5BJD3 | Trypanosoma cruzi | 48% | 100% |