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: A4H5T2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.537 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.586 |
CLV_PCSK_FUR_1 | 306 | 310 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.378 |
DEG_APCC_DBOX_1 | 363 | 371 | PF00400 | 0.379 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.566 |
DEG_SPOP_SBC_1 | 174 | 178 | PF00917 | 0.554 |
DEG_SPOP_SBC_1 | 210 | 214 | PF00917 | 0.386 |
DEG_SPOP_SBC_1 | 315 | 319 | PF00917 | 0.636 |
DOC_CKS1_1 | 27 | 32 | PF01111 | 0.563 |
DOC_MAPK_gen_1 | 219 | 227 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 294 | 302 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 220 | 229 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 364 | 371 | PF00069 | 0.379 |
DOC_MAPK_NFAT4_5 | 364 | 372 | PF00069 | 0.378 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.620 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.810 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 144 | 151 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 157 | 165 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 308 | 316 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 338 | 343 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 352 | 356 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 387 | 393 | PF00244 | 0.504 |
LIG_BRCT_BRCA1_1 | 338 | 342 | PF00533 | 0.549 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.520 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.423 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.505 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.568 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.521 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.572 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.532 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.526 |
LIG_IBAR_NPY_1 | 158 | 160 | PF08397 | 0.629 |
LIG_IRF3_LxIS_1 | 58 | 63 | PF10401 | 0.553 |
LIG_SH2_SRC | 170 | 173 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.514 |
LIG_SH3_1 | 24 | 30 | PF00018 | 0.560 |
LIG_SH3_2 | 27 | 32 | PF14604 | 0.563 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.742 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.641 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.572 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.688 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.466 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.567 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.555 |
LIG_SUMO_SIM_anti_2 | 366 | 371 | PF11976 | 0.379 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.568 |
MOD_CDK_SPK_2 | 259 | 264 | PF00069 | 0.654 |
MOD_CDK_SPxK_1 | 126 | 132 | PF00069 | 0.519 |
MOD_CDK_SPxK_1 | 26 | 32 | PF00069 | 0.561 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.583 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.585 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.502 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.691 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.474 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.639 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.699 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.566 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.387 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.600 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.589 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.618 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.535 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.695 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.457 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.637 |
MOD_GlcNHglycan | 42 | 46 | PF01048 | 0.644 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.607 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.529 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.520 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.525 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.755 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.477 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.642 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.670 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.559 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.523 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.515 |
MOD_N-GLC_1 | 397 | 402 | PF02516 | 0.642 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.650 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.575 |
MOD_NEK2_2 | 388 | 393 | PF00069 | 0.449 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.534 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.476 |
MOD_PKA_1 | 322 | 328 | PF00069 | 0.649 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.594 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.605 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.523 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.643 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.496 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.389 |
MOD_Plk_2-3 | 345 | 351 | PF00069 | 0.426 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.553 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.519 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.808 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.646 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.561 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.542 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.544 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.540 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.551 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.611 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.586 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQV2 | Leishmania donovani | 66% | 100% |
A4HU25 | Leishmania infantum | 65% | 100% |
E9AMV5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
Q4QHS1 | Leishmania major | 63% | 98% |