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: A4HCC4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.616 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.715 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.715 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.448 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.526 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.741 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.768 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.558 |
DOC_CYCLIN_RxL_1 | 345 | 354 | PF00134 | 0.447 |
DOC_MAPK_MEF2A_6 | 484 | 491 | PF00069 | 0.590 |
DOC_PP1_RVXF_1 | 346 | 352 | PF00149 | 0.348 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.695 |
DOC_PP4_FxxP_1 | 294 | 297 | PF00568 | 0.534 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.803 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.760 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 227 | 231 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 268 | 273 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 30 | 35 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 412 | 421 | PF00244 | 0.444 |
LIG_Actin_WH2_2 | 399 | 416 | PF00022 | 0.443 |
LIG_BIR_III_4 | 42 | 46 | PF00653 | 0.585 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.705 |
LIG_CSL_BTD_1 | 438 | 441 | PF09270 | 0.480 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.540 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.555 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.436 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.565 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.628 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.523 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.715 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.785 |
LIG_LIR_Apic_2 | 106 | 111 | PF02991 | 0.688 |
LIG_LIR_Apic_2 | 292 | 297 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 463 | 473 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.445 |
LIG_PDZ_Class_2 | 486 | 491 | PF00595 | 0.455 |
LIG_Pex14_2 | 140 | 144 | PF04695 | 0.474 |
LIG_RPA_C_Fungi | 159 | 171 | PF08784 | 0.587 |
LIG_SH2_NCK_1 | 451 | 455 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 466 | 470 | PF00017 | 0.371 |
LIG_SH2_PTP2 | 339 | 342 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.439 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.609 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.646 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.607 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.535 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.691 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.442 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.458 |
LIG_SUMO_SIM_par_1 | 251 | 258 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 432 | 437 | PF11976 | 0.601 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.581 |
LIG_TYR_ITIM | 464 | 469 | PF00017 | 0.591 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.707 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.603 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.589 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.613 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.437 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.621 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.649 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.731 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.711 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.785 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.704 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.566 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.636 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.576 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.685 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.696 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.629 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.437 |
MOD_GlcNHglycan | 46 | 50 | PF01048 | 0.666 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.578 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.708 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.485 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.681 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.629 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.494 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.634 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.571 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.592 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.765 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.444 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.706 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.564 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.716 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.562 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.496 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.637 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.693 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.493 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.451 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.601 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.440 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.454 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.742 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.441 |
MOD_NEK2_2 | 460 | 465 | PF00069 | 0.414 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.738 |
MOD_PK_1 | 268 | 274 | PF00069 | 0.557 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.571 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.524 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.529 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.424 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.537 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.684 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.439 |
MOD_Plk_2-3 | 73 | 79 | PF00069 | 0.567 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.486 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.631 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.519 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.442 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.437 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.445 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.425 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.567 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.450 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.760 |
TRG_DiLeu_BaEn_2 | 135 | 141 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 345 | 350 | PF01217 | 0.576 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.577 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 348 | 353 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDA8 | Leptomonas seymouri | 46% | 85% |
A0A3Q8IEA0 | Leishmania donovani | 74% | 84% |
A4HZX3 | Leishmania infantum | 74% | 84% |
E9AVT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 84% |
Q4QBP7 | Leishmania major | 75% | 100% |