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: A4HGX3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.647 |
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.558 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.515 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.573 |
CLV_PCSK_PC7_1 | 229 | 235 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.681 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.562 |
DEG_APCC_DBOX_1 | 14 | 22 | PF00400 | 0.575 |
DEG_APCC_DBOX_1 | 174 | 182 | PF00400 | 0.724 |
DEG_APCC_DBOX_1 | 398 | 406 | PF00400 | 0.644 |
DEG_SPOP_SBC_1 | 346 | 350 | PF00917 | 0.722 |
DOC_ANK_TNKS_1 | 278 | 285 | PF00023 | 0.713 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.558 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.692 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.709 |
DOC_USP7_UBL2_3 | 233 | 237 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 65 | 69 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 83 | 87 | PF00244 | 0.598 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.637 |
LIG_BIR_III_2 | 275 | 279 | PF00653 | 0.581 |
LIG_BRCT_MDC1_1 | 433 | 437 | PF00533 | 0.533 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.576 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.438 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.521 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.552 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.448 |
LIG_GBD_Chelix_1 | 94 | 102 | PF00786 | 0.561 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.640 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.667 |
LIG_SUMO_SIM_par_1 | 98 | 105 | PF11976 | 0.576 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.601 |
MOD_CDC14_SPxK_1 | 396 | 399 | PF00782 | 0.651 |
MOD_CDK_SPK_2 | 137 | 142 | PF00069 | 0.671 |
MOD_CDK_SPK_2 | 250 | 255 | PF00069 | 0.617 |
MOD_CDK_SPK_2 | 393 | 398 | PF00069 | 0.661 |
MOD_CDK_SPxK_1 | 393 | 399 | PF00069 | 0.660 |
MOD_CDK_SPxxK_3 | 113 | 120 | PF00069 | 0.666 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.592 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.582 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.710 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.590 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.729 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.609 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.519 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.539 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.578 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.612 |
MOD_CMANNOS | 386 | 389 | PF00535 | 0.686 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.611 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.736 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.563 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.606 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.697 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.666 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.688 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.645 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.631 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.562 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.706 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.583 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.582 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.579 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.708 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.544 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.586 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.652 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.413 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.562 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.617 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.544 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.597 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.638 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.650 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.560 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.710 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.571 |
MOD_PK_1 | 57 | 63 | PF00069 | 0.612 |
MOD_PKA_1 | 341 | 347 | PF00069 | 0.576 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.729 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.585 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.709 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.439 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.566 |
MOD_PKB_1 | 297 | 305 | PF00069 | 0.733 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.633 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.544 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.512 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.599 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.690 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.606 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.671 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.652 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.660 |
TRG_DiLeu_BaEn_4 | 400 | 406 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 326 | 331 | PF01217 | 0.564 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.735 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.716 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 414 | 416 | PF00400 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IID2 | Leishmania donovani | 59% | 94% |
A4I403 | Leishmania infantum | 59% | 94% |
E9B093 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 94% |
Q4Q7Z2 | Leishmania major | 58% | 99% |