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 |
Related structures:
AlphaFold database: A4HJK7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.595 |
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.593 |
CLV_C14_Caspase3-7 | 346 | 350 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.661 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.669 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.627 |
DOC_CDC14_PxL_1 | 38 | 46 | PF14671 | 0.582 |
DOC_CKS1_1 | 17 | 22 | PF01111 | 0.561 |
DOC_SPAK_OSR1_1 | 272 | 276 | PF12202 | 0.583 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.612 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 114 | 123 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 216 | 224 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 272 | 276 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 37 | 42 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.536 |
LIG_Actin_WH2_2 | 415 | 432 | PF00022 | 0.594 |
LIG_Actin_WH2_2 | 94 | 112 | PF00022 | 0.553 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.592 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.649 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.515 |
LIG_Clathr_ClatBox_1 | 58 | 62 | PF01394 | 0.617 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.546 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.585 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.556 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.699 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.586 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.716 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 370 | 379 | PF02991 | 0.645 |
LIG_LIR_LC3C_4 | 56 | 61 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.658 |
LIG_Pex14_1 | 156 | 160 | PF04695 | 0.613 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.546 |
LIG_SH2_NCK_1 | 38 | 42 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.607 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.632 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.612 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.657 |
LIG_SUMO_SIM_anti_2 | 56 | 63 | PF11976 | 0.626 |
LIG_SUMO_SIM_par_1 | 283 | 288 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 56 | 63 | PF11976 | 0.638 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.592 |
LIG_UBA3_1 | 321 | 329 | PF00899 | 0.573 |
LIG_WW_3 | 435 | 439 | PF00397 | 0.750 |
MOD_CDC14_SPxK_1 | 403 | 406 | PF00782 | 0.611 |
MOD_CDK_SPxK_1 | 400 | 406 | PF00069 | 0.614 |
MOD_CDK_SPxxK_3 | 344 | 351 | PF00069 | 0.582 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.575 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.645 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.698 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.581 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.466 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.633 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.558 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.801 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.506 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.691 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.713 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.746 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.595 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.721 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.700 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.802 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.641 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.630 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.612 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.673 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.570 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.697 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.595 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.783 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.657 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.580 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.672 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.601 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.557 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.573 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.565 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.597 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.812 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.773 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.648 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.678 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.599 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.763 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.752 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.680 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.704 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.561 |
MOD_PIKK_1 | 324 | 330 | PF00454 | 0.572 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.608 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.691 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.581 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.546 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.546 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.606 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.612 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.623 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.741 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.548 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.573 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.594 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.561 |
MOD_Plk_2-3 | 135 | 141 | PF00069 | 0.578 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.738 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.729 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.587 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.538 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.561 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.544 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.587 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.548 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.711 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.753 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.630 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.649 |
MOD_SUMO_rev_2 | 346 | 352 | PF00179 | 0.746 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 171 | 175 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 196 | 200 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ50 | Leptomonas seymouri | 33% | 98% |
A0A3S7X4S8 | Leishmania donovani | 52% | 100% |
A4HJK4 | Leishmania braziliensis | 98% | 100% |
A4I706 | Leishmania infantum | 52% | 100% |
E9B224 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
Q4Q638 | Leishmania major | 51% | 100% |