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: A4HD53
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.578 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.541 |
CLV_PCSK_FUR_1 | 246 | 250 | PF00082 | 0.534 |
CLV_PCSK_FUR_1 | 366 | 370 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.536 |
CLV_PCSK_PC7_1 | 177 | 183 | PF00082 | 0.410 |
CLV_PCSK_PC7_1 | 287 | 293 | PF00082 | 0.463 |
CLV_PCSK_PC7_1 | 364 | 370 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.623 |
DEG_APCC_DBOX_1 | 203 | 211 | PF00400 | 0.355 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.681 |
DEG_SPOP_SBC_1 | 46 | 50 | PF00917 | 0.528 |
DOC_CKS1_1 | 139 | 144 | PF01111 | 0.605 |
DOC_CKS1_1 | 347 | 352 | PF01111 | 0.557 |
DOC_CYCLIN_RxL_1 | 366 | 379 | PF00134 | 0.553 |
DOC_MAPK_gen_1 | 364 | 376 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.521 |
DOC_MAPK_RevD_3 | 300 | 314 | PF00069 | 0.342 |
DOC_PP1_RVXF_1 | 265 | 271 | PF00149 | 0.360 |
DOC_PP1_RVXF_1 | 409 | 415 | PF00149 | 0.515 |
DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.526 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.538 |
DOC_USP7_UBL2_3 | 470 | 474 | PF12436 | 0.665 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 166 | 176 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 181 | 190 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 231 | 240 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 366 | 376 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 426 | 432 | PF00244 | 0.456 |
LIG_Actin_WH2_2 | 298 | 315 | PF00022 | 0.342 |
LIG_APCC_ABBA_1 | 374 | 379 | PF00400 | 0.534 |
LIG_BRCT_BRCA1_1 | 294 | 298 | PF00533 | 0.366 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.639 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.669 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.540 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.483 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.564 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.552 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.698 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.568 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.348 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.337 |
LIG_GBD_Chelix_1 | 268 | 276 | PF00786 | 0.359 |
LIG_LIR_Gen_1 | 141 | 151 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.503 |
LIG_LIR_LC3C_4 | 195 | 198 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 303 | 307 | PF02991 | 0.503 |
LIG_Pex14_2 | 323 | 327 | PF04695 | 0.522 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.583 |
LIG_SH2_PTP2 | 421 | 424 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.519 |
LIG_SH3_1 | 429 | 435 | PF00018 | 0.611 |
LIG_SH3_2 | 4 | 9 | PF14604 | 0.617 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.616 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.628 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.611 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.562 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.695 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.528 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.705 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.391 |
LIG_TRAF2_1 | 306 | 309 | PF00917 | 0.332 |
MOD_CDK_SPxxK_3 | 446 | 453 | PF00069 | 0.538 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.553 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.546 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.732 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.604 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.519 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.545 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.624 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.612 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.583 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.350 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.348 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.338 |
MOD_DYRK1A_RPxSP_1 | 93 | 97 | PF00069 | 0.542 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.543 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.558 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.528 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.591 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.495 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.530 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.519 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.548 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.528 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.634 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.621 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.478 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.502 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.720 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.417 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.594 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.555 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.552 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.541 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.600 |
MOD_N-GLC_2 | 386 | 388 | PF02516 | 0.380 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.670 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.554 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.584 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.371 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.523 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.625 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.643 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.539 |
MOD_NEK2_2 | 393 | 398 | PF00069 | 0.534 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.594 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.604 |
MOD_PK_1 | 461 | 467 | PF00069 | 0.506 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.729 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.453 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.580 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.418 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.704 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.528 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.405 |
MOD_PKB_1 | 229 | 237 | PF00069 | 0.532 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.553 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.580 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.539 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.390 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.503 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.537 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.506 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.622 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.560 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.599 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.660 |
MOD_SUMO_rev_2 | 189 | 196 | PF00179 | 0.523 |
MOD_SUMO_rev_2 | 330 | 336 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 360 | 367 | PF00179 | 0.415 |
TRG_DiLeu_BaEn_1 | 192 | 197 | PF01217 | 0.551 |
TRG_DiLeu_BaEn_1 | 202 | 207 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_1 | 339 | 344 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.399 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 366 | 369 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 409 | 412 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.544 |
TRG_ER_diLys_1 | 470 | 474 | PF00400 | 0.665 |
TRG_NLS_MonoExtC_3 | 364 | 369 | PF00514 | 0.412 |
TRG_NLS_MonoExtN_4 | 362 | 369 | PF00514 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 204 | 209 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IC93 | Leishmania donovani | 71% | 100% |
A4I2A8 | Leishmania infantum | 72% | 100% |
E9AYF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 99% |
Q4Q917 | Leishmania major | 71% | 100% |