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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HPU5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.772 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.463 |
DEG_APCC_DBOX_1 | 127 | 135 | PF00400 | 0.476 |
DEG_MDM2_SWIB_1 | 212 | 220 | PF02201 | 0.431 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.516 |
DOC_CYCLIN_RxL_1 | 255 | 266 | PF00134 | 0.467 |
DOC_MAPK_gen_1 | 125 | 131 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 339 | 349 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 367 | 375 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 341 | 349 | PF00069 | 0.448 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.762 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 188 | 195 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 304 | 308 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 356 | 360 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.531 |
LIG_AP_GAE_1 | 117 | 123 | PF02883 | 0.596 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.592 |
LIG_eIF4E_1 | 165 | 171 | PF01652 | 0.442 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.479 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.688 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.527 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.679 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.324 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.491 |
LIG_Integrin_RGD_1 | 86 | 88 | PF01839 | 0.796 |
LIG_LIR_Apic_2 | 73 | 78 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 24 | 34 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.536 |
LIG_NRBOX | 344 | 350 | PF00104 | 0.479 |
LIG_PDZ_Class_3 | 427 | 432 | PF00595 | 0.506 |
LIG_Pex14_2 | 212 | 216 | PF04695 | 0.426 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.501 |
LIG_SH2_GRB2like | 352 | 355 | PF00017 | 0.434 |
LIG_SH2_NCK_1 | 104 | 108 | PF00017 | 0.501 |
LIG_SH2_PTP2 | 352 | 355 | PF00017 | 0.340 |
LIG_SH2_PTP2 | 75 | 78 | PF00017 | 0.491 |
LIG_SH2_SRC | 352 | 355 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.540 |
LIG_SH2_STAT3 | 169 | 172 | PF00017 | 0.531 |
LIG_SH2_STAT3 | 340 | 343 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.606 |
LIG_SH3_1 | 413 | 419 | PF00018 | 0.489 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.750 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.519 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.711 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.489 |
LIG_SUMO_SIM_anti_2 | 147 | 154 | PF11976 | 0.526 |
LIG_SUMO_SIM_anti_2 | 231 | 236 | PF11976 | 0.541 |
LIG_SUMO_SIM_anti_2 | 344 | 349 | PF11976 | 0.419 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.491 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.630 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.705 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.764 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.535 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.618 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.755 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.759 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.588 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.528 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.520 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.559 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.501 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.676 |
MOD_GlcNHglycan | 384 | 388 | PF01048 | 0.575 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.548 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.695 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.714 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.627 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.448 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.455 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.510 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.744 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.736 |
MOD_LATS_1 | 186 | 192 | PF00433 | 0.480 |
MOD_N-GLC_1 | 367 | 372 | PF02516 | 0.538 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.539 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.526 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.458 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.577 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.688 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.740 |
MOD_NEK2_2 | 303 | 308 | PF00069 | 0.591 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.594 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.732 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.785 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.323 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.595 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.549 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.465 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.662 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.773 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.595 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.482 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.702 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.506 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.737 |
TRG_DiLeu_BaEn_1 | 344 | 349 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_4 | 196 | 202 | PF01217 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 252 | 257 | PF01217 | 0.599 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 125 | 128 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 355 | 357 | PF00400 | 0.340 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 199 | 203 | PF00026 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 261 | 265 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 333 | 338 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 413 | 418 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J8 | Leptomonas seymouri | 65% | 100% |
A0A1X0P1T1 | Trypanosomatidae | 57% | 100% |
A0A3Q8ILB9 | Leishmania donovani | 79% | 100% |
A0A422P583 | Trypanosoma rangeli | 55% | 100% |
A4IE48 | Leishmania infantum | 79% | 100% |
E9ATL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q0Y8 | Leishmania major | 79% | 100% |
V5BQ98 | Trypanosoma cruzi | 57% | 100% |