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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4ICV2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.463 |
CLV_PCSK_FUR_1 | 249 | 253 | PF00082 | 0.502 |
CLV_PCSK_FUR_1 | 427 | 431 | PF00082 | 0.553 |
CLV_PCSK_FUR_1 | 45 | 49 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.661 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.688 |
DEG_SCF_FBW7_1 | 442 | 447 | PF00400 | 0.501 |
DEG_SCF_FBW7_2 | 199 | 205 | PF00400 | 0.465 |
DOC_CKS1_1 | 199 | 204 | PF01111 | 0.495 |
DOC_CYCLIN_RxL_1 | 167 | 178 | PF00134 | 0.609 |
DOC_MAPK_gen_1 | 293 | 302 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 212 | 218 | PF00149 | 0.492 |
DOC_PP1_RVXF_1 | 242 | 248 | PF00149 | 0.499 |
DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 264 | 267 | PF13499 | 0.537 |
DOC_PP2B_LxvP_1 | 51 | 54 | PF13499 | 0.653 |
DOC_PP4_FxxP_1 | 62 | 65 | PF00568 | 0.659 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.555 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.497 |
LIG_14-3-3_CanoR_1 | 104 | 109 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 255 | 263 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 411 | 419 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 5 | 13 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 88 | 93 | PF00244 | 0.578 |
LIG_Actin_WH2_2 | 256 | 274 | PF00022 | 0.489 |
LIG_Actin_WH2_2 | 395 | 413 | PF00022 | 0.387 |
LIG_BRCT_BRCA1_1 | 403 | 407 | PF00533 | 0.442 |
LIG_CaM_IQ_9 | 282 | 297 | PF13499 | 0.484 |
LIG_Clathr_ClatBox_1 | 397 | 401 | PF01394 | 0.440 |
LIG_eIF4E_1 | 210 | 216 | PF01652 | 0.500 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.518 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.505 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.601 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.435 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.532 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.373 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.627 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.410 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.526 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 313 | 320 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 386 | 394 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 404 | 415 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 466 | 473 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.442 |
LIG_MAD2 | 115 | 123 | PF02301 | 0.584 |
LIG_Pex14_2 | 217 | 221 | PF04695 | 0.559 |
LIG_PTB_Apo_2 | 472 | 479 | PF02174 | 0.418 |
LIG_PTB_Phospho_1 | 472 | 478 | PF10480 | 0.413 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.499 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.438 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.372 |
LIG_SH2_NCK_1 | 373 | 377 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 373 | 377 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 385 | 389 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 469 | 473 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.615 |
LIG_SH3_1 | 162 | 168 | PF00018 | 0.620 |
LIG_SH3_2 | 165 | 170 | PF14604 | 0.632 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.643 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.660 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.656 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.550 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.511 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.669 |
LIG_TYR_ITIM | 302 | 307 | PF00017 | 0.442 |
LIG_UBA3_1 | 216 | 222 | PF00899 | 0.487 |
LIG_UBA3_1 | 263 | 270 | PF00899 | 0.415 |
LIG_WRC_WIRS_1 | 384 | 389 | PF05994 | 0.377 |
MOD_CDK_SPK_2 | 154 | 159 | PF00069 | 0.643 |
MOD_CDK_SPK_2 | 198 | 203 | PF00069 | 0.558 |
MOD_CDK_SPxxK_3 | 332 | 339 | PF00069 | 0.536 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.732 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.624 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.478 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.616 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.408 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.505 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.508 |
MOD_DYRK1A_RPxSP_1 | 332 | 336 | PF00069 | 0.541 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.629 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.596 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.611 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.581 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.535 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.580 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.431 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.406 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.636 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.524 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.622 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.637 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.496 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.636 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.593 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.495 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.421 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.656 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.436 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.561 |
MOD_LATS_1 | 86 | 92 | PF00433 | 0.545 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.414 |
MOD_N-GLC_2 | 475 | 477 | PF02516 | 0.411 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.751 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.645 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.438 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.395 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.430 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.552 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.414 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.578 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.435 |
MOD_PK_1 | 354 | 360 | PF00069 | 0.526 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.615 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.405 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.476 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.577 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.473 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.615 |
MOD_PKB_1 | 104 | 112 | PF00069 | 0.547 |
MOD_PKB_1 | 352 | 360 | PF00069 | 0.518 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.660 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.622 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.557 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.420 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.526 |
MOD_Plk_2-3 | 369 | 375 | PF00069 | 0.512 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.546 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.445 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.463 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.434 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.335 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.667 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.783 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.587 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.536 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.499 |
MOD_SUMO_rev_2 | 182 | 188 | PF00179 | 0.510 |
MOD_SUMO_rev_2 | 481 | 489 | PF00179 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 352 | 355 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 410 | 412 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 427 | 430 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 450 | 453 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 493 | 496 | PF00400 | 0.492 |
TRG_NLS_Bipartite_1 | 290 | 309 | PF00514 | 0.438 |
TRG_NLS_MonoExtC_3 | 304 | 309 | PF00514 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 170 | 175 | PF00026 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 462 | 466 | PF00026 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IJS5 | Leishmania donovani | 99% | 100% |
A4HNP3 | Leishmania braziliensis | 63% | 100% |
E9ASF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q243 | Leishmania major | 90% | 100% |