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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4HKE0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.643 |
CLV_C14_Caspase3-7 | 436 | 440 | PF00656 | 0.494 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.536 |
CLV_PCSK_FUR_1 | 78 | 82 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.754 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 330 | 332 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 429 | 431 | PF00082 | 0.644 |
CLV_PCSK_PC7_1 | 255 | 261 | PF00082 | 0.643 |
CLV_PCSK_PC7_1 | 326 | 332 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.685 |
DOC_CDC14_PxL_1 | 152 | 160 | PF14671 | 0.390 |
DOC_CDC14_PxL_1 | 421 | 429 | PF14671 | 0.507 |
DOC_CYCLIN_RxL_1 | 407 | 414 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 143 | 152 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 281 | 288 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 52 | 61 | PF00069 | 0.646 |
DOC_PP2B_LxvP_1 | 111 | 114 | PF13499 | 0.520 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.491 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.493 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.391 |
LIG_14-3-3_CanoR_1 | 178 | 187 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 397 | 403 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 410 | 418 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 430 | 438 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 445 | 451 | PF00244 | 0.428 |
LIG_Actin_WH2_2 | 177 | 194 | PF00022 | 0.407 |
LIG_Actin_WH2_2 | 381 | 399 | PF00022 | 0.496 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.646 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.399 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.490 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.412 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.445 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.435 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.653 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 154 | 160 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 372 | 382 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 420 | 427 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 102 | 106 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 420 | 424 | PF02991 | 0.483 |
LIG_MYND_1 | 156 | 160 | PF01753 | 0.500 |
LIG_NRBOX | 408 | 414 | PF00104 | 0.480 |
LIG_PCNA_yPIPBox_3 | 410 | 422 | PF02747 | 0.491 |
LIG_Pex14_1 | 173 | 177 | PF04695 | 0.510 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.503 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.454 |
LIG_SH2_GRB2like | 374 | 377 | PF00017 | 0.407 |
LIG_SH2_PTP2 | 374 | 377 | PF00017 | 0.407 |
LIG_SH2_SRC | 309 | 312 | PF00017 | 0.454 |
LIG_SH2_SRC | 374 | 377 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.684 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.387 |
LIG_SUMO_SIM_par_1 | 131 | 136 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 215 | 221 | PF11976 | 0.481 |
LIG_TYR_ITIM | 175 | 180 | PF00017 | 0.571 |
LIG_TYR_ITIM | 384 | 389 | PF00017 | 0.611 |
LIG_WRC_WIRS_1 | 100 | 105 | PF05994 | 0.247 |
LIG_WRC_WIRS_1 | 418 | 423 | PF05994 | 0.608 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.528 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.422 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.512 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.648 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.480 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.542 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.491 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.565 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.519 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.649 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.603 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.622 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.743 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.622 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.683 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.705 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.671 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.582 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.556 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.638 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.703 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.623 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.624 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.623 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.651 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.755 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.703 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.586 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.547 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.637 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.580 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.640 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.686 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.571 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.574 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.508 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.667 |
MOD_NEK2_2 | 265 | 270 | PF00069 | 0.523 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.445 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.559 |
MOD_PK_1 | 6 | 12 | PF00069 | 0.551 |
MOD_PKA_1 | 429 | 435 | PF00069 | 0.531 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.570 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.531 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.515 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.660 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.551 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.564 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.586 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.532 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.547 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.615 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.247 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.536 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.468 |
MOD_SUMO_for_1 | 208 | 211 | PF00179 | 0.516 |
MOD_SUMO_for_1 | 83 | 86 | PF00179 | 0.609 |
TRG_DiLeu_BaEn_3 | 164 | 170 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 171 | 176 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.657 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.488 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 77 | 80 | PF00400 | 0.697 |
TRG_Pf-PMV_PEXEL_1 | 178 | 183 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 410 | 415 | PF00026 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 44 | 48 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X5J8 | Leishmania donovani | 53% | 88% |
A4I7W8 | Leishmania infantum | 50% | 77% |
E9B2S8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 86% |
Q4Q5C9 | Leishmania major | 52% | 100% |