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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9APU5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.342 |
DEG_APCC_DBOX_1 | 350 | 358 | PF00400 | 0.632 |
DEG_SPOP_SBC_1 | 43 | 47 | PF00917 | 0.671 |
DOC_CYCLIN_yCln2_LP_2 | 203 | 209 | PF00134 | 0.513 |
DOC_CYCLIN_yCln2_LP_2 | 341 | 347 | PF00134 | 0.672 |
DOC_MAPK_gen_1 | 138 | 146 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 208 | 216 | PF00069 | 0.667 |
DOC_MAPK_gen_1 | 349 | 357 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 192 | 200 | PF00069 | 0.238 |
DOC_MAPK_MEF2A_6 | 324 | 332 | PF00069 | 0.425 |
DOC_PP2B_LxvP_1 | 168 | 171 | PF13499 | 0.359 |
DOC_PP2B_LxvP_1 | 355 | 358 | PF13499 | 0.509 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.783 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.845 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.784 |
LIG_14-3-3_CanoR_1 | 116 | 123 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 208 | 218 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 247 | 255 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 26 | 33 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 279 | 284 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.722 |
LIG_Actin_WH2_2 | 193 | 210 | PF00022 | 0.501 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.814 |
LIG_BRCT_BRCA1_1 | 67 | 71 | PF00533 | 0.558 |
LIG_Clathr_ClatBox_1 | 77 | 81 | PF01394 | 0.671 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.300 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.579 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.530 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.752 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.316 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.763 |
LIG_GBD_Chelix_1 | 194 | 202 | PF00786 | 0.238 |
LIG_Integrin_RGD_1 | 13 | 15 | PF01839 | 0.502 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.729 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 421 | 425 | PF02991 | 0.472 |
LIG_NRBOX | 327 | 333 | PF00104 | 0.452 |
LIG_PCNA_yPIPBox_3 | 260 | 268 | PF02747 | 0.531 |
LIG_PTAP_UEV_1 | 425 | 430 | PF05743 | 0.526 |
LIG_RPA_C_Fungi | 187 | 199 | PF08784 | 0.238 |
LIG_SH2_GRB2like | 383 | 386 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 248 | 252 | PF00017 | 0.657 |
LIG_SH2_SRC | 383 | 386 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.575 |
LIG_SH3_1 | 167 | 173 | PF00018 | 0.529 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.577 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.757 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.557 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.723 |
LIG_SUMO_SIM_anti_2 | 54 | 61 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 191 | 197 | PF11976 | 0.296 |
LIG_WRC_WIRS_1 | 148 | 153 | PF05994 | 0.530 |
LIG_WRC_WIRS_1 | 419 | 424 | PF05994 | 0.568 |
LIG_WW_2 | 170 | 173 | PF00397 | 0.450 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.560 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.585 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.530 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.602 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.633 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.372 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.530 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.662 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.780 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.650 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.547 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.663 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.376 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.573 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.647 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.475 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.633 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.530 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.518 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.324 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.644 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.549 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.616 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.316 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.456 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.390 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.590 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.506 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.369 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.511 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.678 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.517 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.727 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.489 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.576 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.611 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.727 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.630 |
MOD_PKB_1 | 26 | 34 | PF00069 | 0.433 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.584 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.530 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.460 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.307 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.530 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.535 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.822 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.462 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.633 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.733 |
TRG_DiLeu_BaLyEn_6 | 414 | 419 | PF01217 | 0.638 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.818 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 348 | 351 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 124 | 129 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I9V0 | Leishmania donovani | 86% | 100% |
A4H7Q3 | Leishmania braziliensis | 73% | 100% |
A4HW42 | Leishmania infantum | 86% | 100% |
Q4QFN5 | Leishmania major | 85% | 100% |