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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AQR6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.603 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.675 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.486 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.447 |
DEG_SPOP_SBC_1 | 196 | 200 | PF00917 | 0.706 |
DOC_MAPK_gen_1 | 144 | 152 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 407 | 417 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 119 | 126 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 410 | 419 | PF00069 | 0.472 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.433 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.416 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 209 | 219 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 222 | 226 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 353 | 359 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 45 | 52 | PF00244 | 0.570 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.585 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.537 |
LIG_CSL_BTD_1 | 87 | 90 | PF09270 | 0.451 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.646 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.506 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.445 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.563 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.605 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.560 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.605 |
LIG_Integrin_RGD_1 | 459 | 461 | PF01839 | 0.595 |
LIG_Integrin_RGD_1 | 472 | 474 | PF01839 | 0.468 |
LIG_LIR_Apic_2 | 381 | 387 | PF02991 | 0.482 |
LIG_LIR_Apic_2 | 84 | 90 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 329 | 340 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 494 | 504 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.312 |
LIG_Pex14_2 | 73 | 77 | PF04695 | 0.547 |
LIG_REV1ctd_RIR_1 | 425 | 435 | PF16727 | 0.300 |
LIG_RPA_C_Fungi | 363 | 375 | PF08784 | 0.388 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.473 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.414 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.566 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.418 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.538 |
LIG_SH2_NCK_1 | 384 | 388 | PF00017 | 0.507 |
LIG_SH2_SRC | 166 | 169 | PF00017 | 0.631 |
LIG_SH2_SRC | 436 | 439 | PF00017 | 0.486 |
LIG_SH2_SRC | 81 | 84 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.360 |
LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.447 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.641 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.643 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 278 | 284 | PF11976 | 0.578 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.481 |
LIG_TRAF2_1 | 357 | 360 | PF00917 | 0.663 |
LIG_TRFH_1 | 498 | 502 | PF08558 | 0.520 |
LIG_TYR_ITIM | 330 | 335 | PF00017 | 0.427 |
LIG_UBA3_1 | 142 | 147 | PF00899 | 0.460 |
LIG_UBA3_1 | 484 | 493 | PF00899 | 0.614 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.481 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.589 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.687 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.693 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.627 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.619 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.561 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.471 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.508 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.517 |
MOD_CMANNOS | 389 | 392 | PF00535 | 0.610 |
MOD_Cter_Amidation | 259 | 262 | PF01082 | 0.477 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.693 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.404 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.455 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.616 |
MOD_GlcNHglycan | 61 | 65 | PF01048 | 0.778 |
MOD_GlcNHglycan | 67 | 71 | PF01048 | 0.714 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.699 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.565 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.708 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.613 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.460 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.509 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.616 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.480 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.391 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.606 |
MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.682 |
MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.644 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.643 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.379 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.669 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.483 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.445 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.336 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.484 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.498 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.624 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.504 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.617 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.680 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.654 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.431 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.693 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.531 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.726 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.628 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.468 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.605 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.738 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.356 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.631 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.378 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.549 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.522 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.724 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.514 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.432 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 359 | 364 | PF00179 | 0.565 |
TRG_DiLeu_BaEn_1 | 231 | 236 | PF01217 | 0.377 |
TRG_DiLeu_BaEn_1 | 275 | 280 | PF01217 | 0.404 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 351 | 353 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 296 | 301 | PF00026 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM4 | Leptomonas seymouri | 69% | 100% |
A0A0S4KPP2 | Bodo saltans | 32% | 100% |
A0A1X0NYW7 | Trypanosomatidae | 42% | 100% |
A0A3S7WU15 | Leishmania donovani | 92% | 98% |
A0A422NAT9 | Trypanosoma rangeli | 43% | 100% |
A4H8N3 | Leishmania braziliensis | 80% | 99% |
A4HX03 | Leishmania infantum | 92% | 98% |
C9ZW04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q4QER0 | Leishmania major | 89% | 100% |