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: A4HEY8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.524 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.562 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.588 |
DEG_APCC_DBOX_1 | 211 | 219 | PF00400 | 0.469 |
DEG_SCF_FBW7_1 | 231 | 238 | PF00400 | 0.534 |
DEG_SPOP_SBC_1 | 426 | 430 | PF00917 | 0.486 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.496 |
DOC_CKS1_1 | 188 | 193 | PF01111 | 0.587 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.480 |
DOC_CYCLIN_RxL_1 | 245 | 253 | PF00134 | 0.356 |
DOC_CYCLIN_yCln2_LP_2 | 114 | 120 | PF00134 | 0.482 |
DOC_MAPK_gen_1 | 245 | 254 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 212 | 219 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 245 | 254 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 427 | 435 | PF00069 | 0.500 |
DOC_MAPK_NFAT4_5 | 212 | 220 | PF00069 | 0.397 |
DOC_PP1_SILK_1 | 269 | 274 | PF00149 | 0.502 |
DOC_PP2B_LxvP_1 | 204 | 207 | PF13499 | 0.397 |
DOC_PP4_FxxP_1 | 188 | 191 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.602 |
LIG_14-3-3_CanoR_1 | 154 | 163 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 239 | 244 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 369 | 378 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 427 | 432 | PF00244 | 0.492 |
LIG_BRCT_BRCA1_1 | 394 | 398 | PF00533 | 0.653 |
LIG_CSL_BTD_1 | 29 | 32 | PF09270 | 0.564 |
LIG_deltaCOP1_diTrp_1 | 28 | 37 | PF00928 | 0.418 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.592 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.489 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.480 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.497 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.415 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.444 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.563 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.608 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.619 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.485 |
LIG_Integrin_RGD_1 | 277 | 279 | PF01839 | 0.576 |
LIG_LIR_Apic_2 | 157 | 163 | PF02991 | 0.566 |
LIG_LIR_Apic_2 | 186 | 191 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 306 | 316 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 33 | 41 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.622 |
LIG_NRBOX | 123 | 129 | PF00104 | 0.519 |
LIG_NRBOX | 214 | 220 | PF00104 | 0.473 |
LIG_PDZ_Class_2 | 430 | 435 | PF00595 | 0.530 |
LIG_Pex14_1 | 34 | 38 | PF04695 | 0.481 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.527 |
LIG_SH2_NCK_1 | 160 | 164 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.472 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.482 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.601 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.715 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.561 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.558 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.534 |
LIG_SUMO_SIM_par_1 | 215 | 221 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 79 | 85 | PF11976 | 0.557 |
LIG_TRAF2_1 | 244 | 247 | PF00917 | 0.555 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.460 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.497 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.545 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.637 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.460 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.455 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.623 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.527 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.533 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.422 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.501 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.549 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.637 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.550 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.575 |
MOD_GlcNHglycan | 279 | 283 | PF01048 | 0.745 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.584 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.499 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.618 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.530 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.416 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.578 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.455 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.498 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.625 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.429 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.627 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.607 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.724 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.499 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.809 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.580 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.607 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.534 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.418 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.436 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.572 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.473 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.602 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.475 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.479 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.511 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.708 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.584 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.460 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.406 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.518 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.563 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.472 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.615 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.557 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.488 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.581 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.490 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.692 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.541 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.660 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.601 |
MOD_SUMO_rev_2 | 371 | 376 | PF00179 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.539 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 248 | 253 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H2 | Leptomonas seymouri | 30% | 100% |
A0A3S7WZZ6 | Leishmania donovani | 64% | 87% |
A4I262 | Leishmania infantum | 64% | 100% |
E9AYB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
Q4Q961 | Leishmania major | 64% | 95% |