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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9B3H2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.450 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.517 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 536 | 538 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.371 |
CLV_PCSK_PC7_1 | 83 | 89 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.483 |
DEG_APCC_DBOX_1 | 147 | 155 | PF00400 | 0.492 |
DEG_APCC_DBOX_1 | 160 | 168 | PF00400 | 0.509 |
DEG_APCC_DBOX_1 | 527 | 535 | PF00400 | 0.472 |
DEG_SCF_FBW7_1 | 74 | 80 | PF00400 | 0.591 |
DOC_CDC14_PxL_1 | 448 | 456 | PF14671 | 0.510 |
DOC_CKS1_1 | 74 | 79 | PF01111 | 0.600 |
DOC_CYCLIN_RxL_1 | 362 | 371 | PF00134 | 0.477 |
DOC_CYCLIN_yCln2_LP_2 | 303 | 309 | PF00134 | 0.458 |
DOC_MAPK_DCC_7 | 172 | 180 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 299 | 309 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 536 | 547 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 540 | 549 | PF00069 | 0.493 |
DOC_MAPK_RevD_3 | 404 | 419 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 416 | 423 | PF00149 | 0.430 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.559 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.556 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 474 | 479 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 516 | 522 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 540 | 549 | PF00244 | 0.262 |
LIG_Actin_WH2_2 | 183 | 200 | PF00022 | 0.508 |
LIG_Actin_WH2_2 | 471 | 489 | PF00022 | 0.405 |
LIG_CaM_NSCaTE_8 | 228 | 235 | PF13499 | 0.451 |
LIG_Clathr_ClatBox_1 | 352 | 356 | PF01394 | 0.375 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.559 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.370 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.347 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.452 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.286 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.462 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.447 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.501 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.403 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.446 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.508 |
LIG_HCF-1_HBM_1 | 371 | 374 | PF13415 | 0.516 |
LIG_LIR_Gen_1 | 22 | 30 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 253 | 263 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 266 | 276 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 308 | 318 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 371 | 382 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.443 |
LIG_LYPXL_yS_3 | 381 | 384 | PF13949 | 0.388 |
LIG_MYND_1 | 551 | 555 | PF01753 | 0.598 |
LIG_NRBOX | 130 | 136 | PF00104 | 0.538 |
LIG_NRBOX | 505 | 511 | PF00104 | 0.487 |
LIG_PCNA_PIPBox_1 | 367 | 376 | PF02747 | 0.550 |
LIG_PCNA_yPIPBox_3 | 249 | 263 | PF02747 | 0.460 |
LIG_PCNA_yPIPBox_3 | 365 | 374 | PF02747 | 0.439 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.418 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.438 |
LIG_SH2_SRC | 36 | 39 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.503 |
LIG_SH2_STAT3 | 376 | 379 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.528 |
LIG_SH3_2 | 74 | 79 | PF14604 | 0.545 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.489 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.439 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 350 | 357 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 425 | 430 | PF11976 | 0.277 |
LIG_SUMO_SIM_par_1 | 211 | 216 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 350 | 357 | PF11976 | 0.345 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.474 |
LIG_TYR_ITIM | 63 | 68 | PF00017 | 0.409 |
LIG_UBA3_1 | 218 | 227 | PF00899 | 0.488 |
LIG_UBA3_1 | 359 | 366 | PF00899 | 0.494 |
LIG_UBA3_1 | 506 | 511 | PF00899 | 0.382 |
LIG_UBA3_1 | 530 | 536 | PF00899 | 0.403 |
LIG_UBA3_1 | 63 | 69 | PF00899 | 0.268 |
MOD_CDK_SPxK_1 | 73 | 79 | PF00069 | 0.630 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.535 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.466 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.513 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.469 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.479 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.404 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.469 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.514 |
MOD_DYRK1A_RPxSP_1 | 8 | 12 | PF00069 | 0.530 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.567 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.487 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.381 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.552 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.519 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.311 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.398 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.457 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.431 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.441 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.201 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.401 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.445 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.425 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.437 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.439 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.543 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.558 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.552 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.230 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.422 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.480 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.223 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.466 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.247 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.442 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.400 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.359 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.578 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.440 |
MOD_NEK2_2 | 517 | 522 | PF00069 | 0.528 |
MOD_PIKK_1 | 540 | 546 | PF00454 | 0.247 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.443 |
MOD_PK_1 | 474 | 480 | PF00069 | 0.479 |
MOD_PKA_1 | 536 | 542 | PF00069 | 0.405 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.545 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.663 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.405 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.520 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.554 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.560 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.500 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.525 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.481 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.414 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.341 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.483 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.387 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.335 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.456 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.459 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.554 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.606 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 136 | 141 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 209 | 214 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 525 | 530 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.409 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 514 | 516 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 100 | 104 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 287 | 291 | PF00026 | 0.674 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II47 | Leptomonas seymouri | 58% | 100% |
A0A0S4JG92 | Bodo saltans | 23% | 76% |
A0A1X0NRZ6 | Trypanosomatidae | 39% | 99% |
A0A3Q8IGL6 | Leishmania donovani | 92% | 100% |
A0A422NHU1 | Trypanosoma rangeli | 41% | 98% |
A4HL31 | Leishmania braziliensis | 80% | 100% |
A4I8L2 | Leishmania infantum | 91% | 100% |
D0AAK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 92% |
Q4Q4M8 | Leishmania major | 92% | 100% |
V5BI03 | Trypanosoma cruzi | 41% | 98% |