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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HGB8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.355 |
DEG_APCC_DBOX_1 | 333 | 341 | PF00400 | 0.580 |
DOC_CYCLIN_RxL_1 | 109 | 117 | PF00134 | 0.500 |
DOC_CYCLIN_RxL_1 | 202 | 212 | PF00134 | 0.283 |
DOC_CYCLIN_yCln2_LP_2 | 96 | 102 | PF00134 | 0.619 |
DOC_PP1_RVXF_1 | 110 | 116 | PF00149 | 0.500 |
DOC_PP1_RVXF_1 | 183 | 190 | PF00149 | 0.284 |
DOC_PP1_RVXF_1 | 221 | 228 | PF00149 | 0.447 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.392 |
DOC_PP4_FxxP_1 | 35 | 38 | PF00568 | 0.641 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.681 |
DOC_USP7_UBL2_3 | 40 | 44 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.287 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.260 |
LIG_14-3-3_CanoR_1 | 351 | 355 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 383 | 389 | PF00244 | 0.681 |
LIG_APCC_ABBA_1 | 422 | 427 | PF00400 | 0.831 |
LIG_BIR_III_4 | 443 | 447 | PF00653 | 0.583 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.419 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.447 |
LIG_Clathr_ClatBox_1 | 56 | 60 | PF01394 | 0.682 |
LIG_deltaCOP1_diTrp_1 | 128 | 137 | PF00928 | 0.407 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.462 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.296 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.729 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.756 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.646 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.389 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.737 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.680 |
LIG_GBD_Chelix_1 | 106 | 114 | PF00786 | 0.500 |
LIG_LIR_Apic_2 | 33 | 38 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 25 | 34 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 386 | 397 | PF02991 | 0.697 |
LIG_LIR_Gen_1 | 431 | 442 | PF02991 | 0.721 |
LIG_LIR_Gen_1 | 58 | 64 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 25 | 29 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.725 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.736 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.552 |
LIG_MYND_1 | 99 | 103 | PF01753 | 0.555 |
LIG_NRBOX | 105 | 111 | PF00104 | 0.500 |
LIG_Pex14_2 | 263 | 267 | PF04695 | 0.391 |
LIG_PTB_Apo_2 | 29 | 36 | PF02174 | 0.581 |
LIG_REV1ctd_RIR_1 | 264 | 272 | PF16727 | 0.436 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.770 |
LIG_SH2_NCK_1 | 389 | 393 | PF00017 | 0.609 |
LIG_SH2_STAT3 | 20 | 23 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.676 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.577 |
LIG_SH3_4 | 37 | 44 | PF00018 | 0.680 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.428 |
LIG_TRAF2_1 | 456 | 459 | PF00917 | 0.752 |
LIG_WRC_WIRS_1 | 263 | 268 | PF05994 | 0.427 |
LIG_WRC_WIRS_1 | 299 | 304 | PF05994 | 0.300 |
LIG_WRC_WIRS_1 | 56 | 61 | PF05994 | 0.496 |
MOD_CDK_SPK_2 | 180 | 185 | PF00069 | 0.287 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.379 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.329 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.357 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.430 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.726 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.776 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.845 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.390 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.604 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.701 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.724 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.636 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.662 |
MOD_GlcNHglycan | 147 | 151 | PF01048 | 0.586 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.632 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.644 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.577 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.488 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.465 |
MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.453 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.532 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.486 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.501 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.438 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.436 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.398 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.607 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.525 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.680 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.714 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.680 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.459 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.665 |
MOD_N-GLC_2 | 194 | 196 | PF02516 | 0.478 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.343 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.325 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.419 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.390 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.449 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.345 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.444 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.596 |
MOD_PKA_1 | 370 | 376 | PF00069 | 0.769 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.422 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.687 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.687 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.677 |
MOD_PKB_1 | 368 | 376 | PF00069 | 0.764 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.493 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.373 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.753 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.789 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.659 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.704 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.434 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.393 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.576 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.606 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.773 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.285 |
MOD_SUMO_rev_2 | 324 | 331 | PF00179 | 0.695 |
MOD_SUMO_rev_2 | 474 | 480 | PF00179 | 0.604 |
TRG_DiLeu_BaEn_1 | 77 | 82 | PF01217 | 0.591 |
TRG_DiLeu_BaEn_1 | 97 | 102 | PF01217 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 96 | 101 | PF01217 | 0.626 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.775 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.759 |
TRG_ER_diLys_1 | 478 | 481 | PF00400 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 112 | 116 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 464 | 468 | PF00026 | 0.436 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PES7 | Leptomonas seymouri | 37% | 100% |
A0A1X0NYH6 | Trypanosomatidae | 24% | 85% |
A0A3Q8ID12 | Leishmania donovani | 74% | 100% |
A4I3F2 | Leishmania infantum | 74% | 100% |
E9AZN9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q8J2 | Leishmania major | 76% | 100% |