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: A4HKC0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 130 | 134 | PF00656 | 0.525 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.476 |
CLV_PCSK_FUR_1 | 345 | 349 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.422 |
DEG_APCC_DBOX_1 | 521 | 529 | PF00400 | 0.373 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.463 |
DEG_SCF_FBW7_2 | 397 | 404 | PF00400 | 0.441 |
DOC_CDC14_PxL_1 | 378 | 386 | PF14671 | 0.483 |
DOC_CKS1_1 | 183 | 188 | PF01111 | 0.562 |
DOC_CYCLIN_RxL_1 | 74 | 86 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 246 | 252 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 265 | 271 | PF00134 | 0.510 |
DOC_PP2B_LxvP_1 | 144 | 147 | PF13499 | 0.551 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.757 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.458 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.427 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.837 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.445 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 256 | 262 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 360 | 365 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 505 | 511 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 66 | 70 | PF00244 | 0.590 |
LIG_BIR_III_2 | 107 | 111 | PF00653 | 0.502 |
LIG_EVH1_2 | 155 | 159 | PF00568 | 0.563 |
LIG_EVH1_2 | 323 | 327 | PF00568 | 0.530 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.626 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.502 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.373 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.531 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.517 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.554 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.495 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.461 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.541 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.463 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.330 |
LIG_KLC1_Yacidic_2 | 498 | 502 | PF13176 | 0.392 |
LIG_LIR_Gen_1 | 16 | 25 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 242 | 252 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 426 | 435 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 240 | 244 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.595 |
LIG_PDZ_Class_2 | 547 | 552 | PF00595 | 0.611 |
LIG_Pex14_1 | 429 | 433 | PF04695 | 0.540 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.445 |
LIG_SH2_GRB2like | 19 | 22 | PF00017 | 0.430 |
LIG_SH2_SRC | 500 | 503 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 294 | 298 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.400 |
LIG_SH3_1 | 145 | 151 | PF00018 | 0.693 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.609 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.626 |
LIG_SH3_CIN85_PxpxPR_1 | 106 | 111 | PF14604 | 0.411 |
LIG_SH3_CIN85_PxpxPR_1 | 249 | 254 | PF14604 | 0.530 |
LIG_SUMO_SIM_anti_2 | 57 | 66 | PF11976 | 0.499 |
LIG_TRAF2_1 | 172 | 175 | PF00917 | 0.559 |
LIG_TRAF2_1 | 434 | 437 | PF00917 | 0.588 |
LIG_UBA3_1 | 44 | 49 | PF00899 | 0.476 |
LIG_UBA3_1 | 528 | 536 | PF00899 | 0.369 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.693 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.532 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.493 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.450 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.748 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.524 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.453 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.583 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.439 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.535 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.447 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.323 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.665 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.668 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.525 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.359 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.719 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.763 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.604 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.602 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.446 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.580 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.549 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.523 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.462 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.287 |
MOD_LATS_1 | 494 | 500 | PF00433 | 0.466 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.530 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.532 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.730 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.706 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.599 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.702 |
MOD_PKA_1 | 504 | 510 | PF00069 | 0.364 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.768 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.517 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.481 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.459 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.393 |
MOD_PKB_1 | 72 | 80 | PF00069 | 0.485 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.585 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.618 |
MOD_Plk_2-3 | 127 | 133 | PF00069 | 0.615 |
MOD_Plk_2-3 | 541 | 547 | PF00069 | 0.429 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.397 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.368 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.696 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.838 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.444 |
MOD_SUMO_for_1 | 409 | 412 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 430 | 439 | PF00179 | 0.525 |
MOD_SUMO_rev_2 | 498 | 506 | PF00179 | 0.523 |
MOD_SUMO_rev_2 | 86 | 94 | PF00179 | 0.472 |
TRG_DiLeu_BaEn_1 | 60 | 65 | PF01217 | 0.496 |
TRG_DiLeu_BaLyEn_6 | 462 | 467 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.681 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 253 | 256 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 256 | 261 | PF00026 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IKZ7 | Leishmania donovani | 69% | 100% |
A4I7U9 | Leishmania infantum | 69% | 100% |
D0AA07 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 97% |
E9B2Q7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
Q4Q5F0 | Leishmania major | 68% | 100% |