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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AVV9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.622 |
CLV_C14_Caspase3-7 | 451 | 455 | PF00656 | 0.727 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.603 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.787 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.742 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 309 | 311 | PF00082 | 0.693 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.465 |
DOC_ANK_TNKS_1 | 218 | 225 | PF00023 | 0.520 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.466 |
DOC_MAPK_gen_1 | 20 | 30 | PF00069 | 0.535 |
DOC_PP1_RVXF_1 | 80 | 86 | PF00149 | 0.470 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.614 |
DOC_PP4_FxxP_1 | 184 | 187 | PF00568 | 0.542 |
DOC_PP4_FxxP_1 | 233 | 236 | PF00568 | 0.674 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.471 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.468 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 158 | 162 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 201 | 210 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 442 | 447 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 55 | 60 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 82 | 86 | PF00244 | 0.482 |
LIG_BIR_III_4 | 493 | 497 | PF00653 | 0.559 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.487 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.589 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.699 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.697 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.489 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.670 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.653 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.723 |
LIG_Integrin_RGD_1 | 216 | 218 | PF01839 | 0.658 |
LIG_LIR_Apic_2 | 232 | 236 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 256 | 261 | PF02991 | 0.657 |
LIG_LIR_Gen_1 | 57 | 68 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.471 |
LIG_PCNA_yPIPBox_3 | 524 | 538 | PF02747 | 0.694 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.462 |
LIG_REV1ctd_RIR_1 | 181 | 186 | PF16727 | 0.590 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.318 |
LIG_SH2_CRK | 60 | 64 | PF00017 | 0.483 |
LIG_SH2_NCK_1 | 60 | 64 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 142 | 145 | PF00017 | 0.560 |
LIG_SH2_STAT3 | 286 | 289 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.711 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.530 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.509 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.692 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.525 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.529 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.456 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.809 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.653 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.456 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.481 |
LIG_SUMO_SIM_anti_2 | 113 | 119 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 456 | 466 | PF11976 | 0.670 |
LIG_SUMO_SIM_par_1 | 529 | 535 | PF11976 | 0.681 |
LIG_UBA3_1 | 347 | 352 | PF00899 | 0.632 |
LIG_WRC_WIRS_1 | 230 | 235 | PF05994 | 0.425 |
MOD_CDK_SPxK_1 | 102 | 108 | PF00069 | 0.477 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.522 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.527 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.767 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.706 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.484 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.557 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.609 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.752 |
MOD_Cter_Amidation | 1 | 4 | PF01082 | 0.508 |
MOD_Cter_Amidation | 149 | 152 | PF01082 | 0.616 |
MOD_DYRK1A_RPxSP_1 | 40 | 44 | PF00069 | 0.458 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.768 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.527 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.699 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.685 |
MOD_GlcNHglycan | 300 | 305 | PF01048 | 0.694 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.778 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.650 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.479 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.744 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.595 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.734 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.766 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.463 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.462 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.477 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.541 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.496 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.672 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.717 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.479 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.519 |
MOD_OFUCOSY | 92 | 98 | PF10250 | 0.467 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.482 |
MOD_PKA_1 | 309 | 315 | PF00069 | 0.680 |
MOD_PKA_1 | 357 | 363 | PF00069 | 0.692 |
MOD_PKA_1 | 442 | 448 | PF00069 | 0.830 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.520 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.527 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.524 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.654 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.680 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.540 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.782 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.459 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.454 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.469 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.592 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.526 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.535 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.426 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.616 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.464 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.715 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.439 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.466 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.560 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.461 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.756 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.488 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.468 |
MOD_SUMO_for_1 | 356 | 359 | PF00179 | 0.664 |
TRG_DiLeu_BaLyEn_6 | 343 | 348 | PF01217 | 0.692 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 322 | 326 | PF00026 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 529 | 534 | PF00026 | 0.687 |
TRG_Pf-PMV_PEXEL_1 | 538 | 542 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICB1 | Leishmania donovani | 90% | 100% |
A4HCG8 | Leishmania braziliensis | 75% | 99% |
E9AGZ7 | Leishmania infantum | 89% | 100% |
Q4QBM0 | Leishmania major | 88% | 100% |