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: A4HMB9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.501 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.474 |
CLV_PCSK_FUR_1 | 387 | 391 | PF00082 | 0.537 |
CLV_PCSK_FUR_1 | 506 | 510 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 451 | 453 | PF00082 | 0.662 |
CLV_PCSK_PC7_1 | 506 | 512 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.583 |
CLV_Separin_Metazoa | 114 | 118 | PF03568 | 0.466 |
DEG_APCC_DBOX_1 | 13 | 21 | PF00400 | 0.604 |
DEG_APCC_DBOX_1 | 139 | 147 | PF00400 | 0.606 |
DEG_APCC_DBOX_1 | 378 | 386 | PF00400 | 0.677 |
DEG_SPOP_SBC_1 | 132 | 136 | PF00917 | 0.400 |
DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.635 |
DOC_CYCLIN_yCln2_LP_2 | 459 | 465 | PF00134 | 0.476 |
DOC_MAPK_gen_1 | 457 | 465 | PF00069 | 0.469 |
DOC_MAPK_RevD_3 | 290 | 303 | PF00069 | 0.654 |
DOC_PP2B_LxvP_1 | 227 | 230 | PF13499 | 0.494 |
DOC_PP4_FxxP_1 | 490 | 493 | PF00568 | 0.572 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.698 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 160 | 167 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 379 | 383 | PF00244 | 0.585 |
LIG_14-3-3_CterR_2 | 517 | 520 | PF00244 | 0.699 |
LIG_Actin_WH2_2 | 364 | 381 | PF00022 | 0.558 |
LIG_APCC_ABBA_1 | 219 | 224 | PF00400 | 0.380 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.551 |
LIG_CtBP_PxDLS_1 | 291 | 295 | PF00389 | 0.708 |
LIG_DLG_GKlike_1 | 65 | 72 | PF00625 | 0.704 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.575 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.632 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.623 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.643 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.590 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.749 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.622 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.586 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.621 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.700 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.572 |
LIG_LIR_Gen_1 | 125 | 133 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 220 | 230 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 76 | 83 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.642 |
LIG_NBox_RRM_1 | 398 | 408 | PF00076 | 0.568 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.585 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.626 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.686 |
LIG_SH2_STAT3 | 267 | 270 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.594 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.707 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.608 |
LIG_SUMO_SIM_par_1 | 177 | 184 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 216 | 224 | PF11976 | 0.628 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.574 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.510 |
LIG_WW_3 | 484 | 488 | PF00397 | 0.523 |
MOD_CDK_SPxK_1 | 434 | 440 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 133 | 140 | PF00069 | 0.610 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.616 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.615 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.632 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.558 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.515 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.525 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.570 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.517 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.636 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.588 |
MOD_Cter_Amidation | 506 | 509 | PF01082 | 0.667 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.433 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.593 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.608 |
MOD_GlcNHglycan | 321 | 325 | PF01048 | 0.661 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.583 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.635 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.466 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.624 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.590 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.635 |
MOD_LATS_1 | 416 | 422 | PF00433 | 0.505 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.673 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.636 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.632 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.643 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.553 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.609 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.647 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.408 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.695 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.473 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.568 |
MOD_PKA_1 | 159 | 165 | PF00069 | 0.412 |
MOD_PKA_1 | 389 | 395 | PF00069 | 0.621 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.639 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.512 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.730 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.592 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.621 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.711 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.691 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.678 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.530 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.556 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.625 |
MOD_Plk_2-3 | 197 | 203 | PF00069 | 0.426 |
MOD_Plk_2-3 | 307 | 313 | PF00069 | 0.585 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.537 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.540 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.585 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.621 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.616 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.542 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.777 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.617 |
MOD_SUMO_for_1 | 343 | 346 | PF00179 | 0.781 |
MOD_SUMO_for_1 | 388 | 391 | PF00179 | 0.634 |
MOD_SUMO_for_1 | 44 | 47 | PF00179 | 0.362 |
MOD_SUMO_rev_2 | 258 | 265 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 27 | 34 | PF00179 | 0.615 |
MOD_SUMO_rev_2 | 421 | 431 | PF00179 | 0.706 |
MOD_SUMO_rev_2 | 432 | 437 | PF00179 | 0.692 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.606 |
TRG_ER_diArg_1 | 107 | 109 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 378 | 380 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 509 | 511 | PF00400 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0N1 | Leptomonas seymouri | 53% | 90% |
A0A1X0NJ03 | Trypanosomatidae | 30% | 89% |
A0A3S7X8Y2 | Leishmania donovani | 78% | 100% |
A0A422NI80 | Trypanosoma rangeli | 33% | 92% |
A4IAY5 | Leishmania infantum | 78% | 100% |
C9ZNI2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 89% |
E9AER3 | Leishmania major | 77% | 100% |
E9B5W8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |