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: E9AWN7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 176 | 180 | PF00656 | 0.688 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.739 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.681 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.487 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.492 |
DOC_CDC14_PxL_1 | 258 | 266 | PF14671 | 0.571 |
DOC_CKS1_1 | 284 | 289 | PF01111 | 0.716 |
DOC_MAPK_gen_1 | 230 | 239 | PF00069 | 0.716 |
DOC_MAPK_gen_1 | 64 | 71 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 64 | 71 | PF00069 | 0.524 |
DOC_PP4_FxxP_1 | 246 | 249 | PF00568 | 0.743 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.790 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.814 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.656 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 234 | 240 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 385 | 394 | PF00244 | 0.783 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.629 |
LIG_Actin_WH2_2 | 249 | 267 | PF00022 | 0.464 |
LIG_Actin_WH2_2 | 54 | 72 | PF00022 | 0.496 |
LIG_APCC_ABBA_1 | 97 | 102 | PF00400 | 0.525 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.518 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.694 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.634 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.496 |
LIG_Clathr_ClatBox_1 | 43 | 47 | PF01394 | 0.443 |
LIG_DLG_GKlike_1 | 312 | 320 | PF00625 | 0.518 |
LIG_DLG_GKlike_1 | 373 | 381 | PF00625 | 0.719 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.508 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.595 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.566 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.567 |
LIG_LIR_Apic_2 | 199 | 205 | PF02991 | 0.652 |
LIG_LIR_Apic_2 | 294 | 299 | PF02991 | 0.689 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 250 | 261 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.499 |
LIG_MLH1_MIPbox_1 | 334 | 338 | PF16413 | 0.496 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.672 |
LIG_SH2_NCK_1 | 175 | 179 | PF00017 | 0.619 |
LIG_SH2_PTP2 | 268 | 271 | PF00017 | 0.736 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.634 |
LIG_SH3_1 | 328 | 334 | PF00018 | 0.717 |
LIG_SH3_2 | 225 | 230 | PF14604 | 0.500 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.590 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.680 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.554 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.711 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.529 |
LIG_SUMO_SIM_anti_2 | 42 | 47 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 42 | 47 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 57 | 63 | PF11976 | 0.449 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.680 |
LIG_WW_3 | 297 | 301 | PF00397 | 0.580 |
MOD_CDK_SPxK_1 | 294 | 300 | PF00069 | 0.761 |
MOD_CDK_SPxxK_3 | 394 | 401 | PF00069 | 0.578 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.661 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.664 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.670 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.782 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.629 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.724 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.501 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.732 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.566 |
MOD_Cter_Amidation | 370 | 373 | PF01082 | 0.537 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.542 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.631 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.741 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.620 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.695 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.728 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.560 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.700 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.788 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.667 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.759 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.621 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.762 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.744 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.749 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.506 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.479 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.738 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.725 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.493 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.535 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.487 |
MOD_NEK2_2 | 380 | 385 | PF00069 | 0.530 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.593 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.693 |
MOD_PKB_1 | 136 | 144 | PF00069 | 0.497 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.472 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.539 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.490 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.670 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.788 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.529 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.658 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.620 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.684 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.704 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.748 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.762 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.636 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.705 |
TRG_DiLeu_BaLyEn_6 | 274 | 279 | PF01217 | 0.478 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.616 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.678 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEP2 | Leptomonas seymouri | 37% | 100% |
A0A3S7WY45 | Leishmania donovani | 86% | 100% |
A4HDU6 | Leishmania braziliensis | 62% | 100% |
A4I0N7 | Leishmania infantum | 87% | 100% |
Q4QAT4 | Leishmania major | 85% | 100% |