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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HDC8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.604 |
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.441 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.666 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.763 |
CLV_PCSK_PC7_1 | 396 | 402 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.647 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.512 |
DEG_APCC_DBOX_1 | 345 | 353 | PF00400 | 0.636 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.502 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.498 |
DOC_CDC14_PxL_1 | 408 | 416 | PF14671 | 0.424 |
DOC_CKS1_1 | 24 | 29 | PF01111 | 0.510 |
DOC_CKS1_1 | 60 | 65 | PF01111 | 0.637 |
DOC_CYCLIN_yCln2_LP_2 | 11 | 17 | PF00134 | 0.463 |
DOC_CYCLIN_yCln2_LP_2 | 115 | 121 | PF00134 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 24 | 30 | PF00134 | 0.422 |
DOC_MAPK_DCC_7 | 164 | 172 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 396 | 405 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 133 | 140 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 164 | 172 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 99 | 107 | PF00069 | 0.639 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.453 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.503 |
DOC_PP4_FxxP_1 | 131 | 134 | PF00568 | 0.409 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.623 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.595 |
LIG_14-3-3_CanoR_1 | 122 | 132 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.493 |
LIG_eIF4E_1 | 19 | 25 | PF01652 | 0.476 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.480 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.476 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.582 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.418 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.527 |
LIG_LIR_Apic_2 | 189 | 194 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 159 | 170 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 77 | 87 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.657 |
LIG_NRBOX | 257 | 263 | PF00104 | 0.534 |
LIG_SH2_NCK_1 | 237 | 241 | PF00017 | 0.593 |
LIG_SH2_SRC | 288 | 291 | PF00017 | 0.667 |
LIG_SH2_STAP1 | 288 | 292 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 366 | 370 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.760 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.554 |
LIG_SH3_1 | 152 | 158 | PF00018 | 0.328 |
LIG_SH3_2 | 168 | 173 | PF14604 | 0.510 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.664 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.449 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.503 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.546 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.716 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.467 |
LIG_SUMO_SIM_par_1 | 104 | 111 | PF11976 | 0.465 |
LIG_UBA3_1 | 24 | 29 | PF00899 | 0.470 |
LIG_WRC_WIRS_1 | 417 | 422 | PF05994 | 0.591 |
MOD_CDK_SPxK_1 | 23 | 29 | PF00069 | 0.607 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.684 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.582 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.483 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.433 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.454 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.594 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.650 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.713 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.474 |
MOD_Cter_Amidation | 320 | 323 | PF01082 | 0.785 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.552 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.577 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.757 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.618 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.789 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.489 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.645 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.726 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.468 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.479 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.599 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.691 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.439 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.451 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.601 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.564 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.632 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.621 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.707 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.549 |
MOD_N-GLC_2 | 306 | 308 | PF02516 | 0.721 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.567 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.548 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.559 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.513 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.494 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.487 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.577 |
MOD_PK_1 | 313 | 319 | PF00069 | 0.623 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.488 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.581 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.684 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.644 |
MOD_PKB_1 | 176 | 184 | PF00069 | 0.462 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.413 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.509 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.496 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.590 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.620 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.566 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.711 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.459 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.635 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.639 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.465 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.586 |
TRG_AP2beta_CARGO_1 | 142 | 152 | PF09066 | 0.326 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.783 |
TRG_DiLeu_BaEn_1 | 230 | 235 | PF01217 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 133 | 138 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 375 | 380 | PF01217 | 0.487 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.594 |
TRG_NES_CRM1_1 | 147 | 159 | PF08389 | 0.462 |
TRG_NLS_MonoExtC_3 | 395 | 400 | PF00514 | 0.490 |
TRG_NLS_MonoExtN_4 | 393 | 400 | PF00514 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.770 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3F4 | Leptomonas seymouri | 41% | 100% |
A0A3S7WY61 | Leishmania donovani | 72% | 100% |
A4I0Q9 | Leishmania infantum | 72% | 100% |
E9AWR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4QAR2 | Leishmania major | 73% | 100% |