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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QAR2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 337 | 341 | PF00656 | 0.452 |
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.495 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.501 |
CLV_PCSK_FUR_1 | 390 | 394 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.412 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.395 |
DEG_APCC_DBOX_1 | 347 | 355 | PF00400 | 0.492 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.541 |
DOC_CKS1_1 | 62 | 67 | PF01111 | 0.557 |
DOC_CYCLIN_RxL_1 | 28 | 37 | PF00134 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 117 | 123 | PF00134 | 0.357 |
DOC_MAPK_DCC_7 | 103 | 112 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 31 | 40 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 103 | 112 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 135 | 142 | PF00069 | 0.383 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.392 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.480 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.547 |
LIG_14-3-3_CanoR_1 | 20 | 29 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 366 | 375 | PF00244 | 0.615 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.555 |
LIG_CaM_NSCaTE_8 | 82 | 89 | PF13499 | 0.471 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.389 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.444 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.496 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.598 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.464 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.586 |
LIG_LIR_LC3C_4 | 6 | 10 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.540 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.543 |
LIG_SH2_SRC | 290 | 293 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.562 |
LIG_SH3_2 | 170 | 175 | PF14604 | 0.396 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.523 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.338 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.391 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.552 |
LIG_SUMO_SIM_anti_2 | 6 | 11 | PF11976 | 0.538 |
LIG_SUMO_SIM_par_1 | 106 | 113 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 6 | 11 | PF11976 | 0.538 |
LIG_WRC_WIRS_1 | 419 | 424 | PF05994 | 0.474 |
MOD_CDK_SPK_2 | 61 | 66 | PF00069 | 0.502 |
MOD_CDK_SPxK_1 | 25 | 31 | PF00069 | 0.544 |
MOD_CDK_SPxxK_3 | 61 | 68 | PF00069 | 0.550 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.557 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.474 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.490 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.511 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.474 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.719 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.600 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.493 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.431 |
MOD_Cter_Amidation | 322 | 325 | PF01082 | 0.631 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.537 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.531 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.622 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.536 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.474 |
MOD_GlcNHglycan | 228 | 232 | PF01048 | 0.490 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.603 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.554 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.580 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.462 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.392 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.620 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.570 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.476 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.334 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.498 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.565 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.537 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.564 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.640 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.635 |
MOD_N-GLC_2 | 308 | 310 | PF02516 | 0.585 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.578 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.450 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.455 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.456 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.437 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.497 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.473 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.436 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.448 |
MOD_PK_1 | 93 | 99 | PF00069 | 0.500 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.493 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.483 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.562 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.536 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.492 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.496 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.597 |
MOD_Plk_2-3 | 384 | 390 | PF00069 | 0.439 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.539 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.471 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.437 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.406 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.547 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.537 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.370 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.506 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.446 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.548 |
MOD_SUMO_for_1 | 217 | 220 | PF00179 | 0.503 |
TRG_DiLeu_BaEn_1 | 222 | 227 | PF01217 | 0.536 |
TRG_DiLeu_BaEn_1 | 232 | 237 | PF01217 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 377 | 382 | PF01217 | 0.390 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.541 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.546 |
TRG_NES_CRM1_1 | 149 | 161 | PF08389 | 0.346 |
TRG_NLS_MonoExtN_4 | 399 | 405 | PF00514 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 224 | 228 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3F4 | Leptomonas seymouri | 43% | 100% |
A0A3S7WY61 | Leishmania donovani | 90% | 100% |
A4HDC8 | Leishmania braziliensis | 73% | 100% |
A4I0Q9 | Leishmania infantum | 90% | 100% |
E9AWR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |