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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AXF5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 169 | 173 | PF00656 | 0.519 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.675 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.485 |
DEG_APCC_DBOX_1 | 163 | 171 | PF00400 | 0.492 |
DEG_APCC_DBOX_1 | 268 | 276 | PF00400 | 0.465 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.512 |
DOC_CYCLIN_RxL_1 | 132 | 142 | PF00134 | 0.314 |
DOC_CYCLIN_RxL_1 | 267 | 277 | PF00134 | 0.522 |
DOC_CYCLIN_yClb1_LxF_4 | 207 | 213 | PF00134 | 0.378 |
DOC_MAPK_FxFP_2 | 211 | 214 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 116 | 123 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 269 | 275 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 32 | 40 | PF00069 | 0.446 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.552 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.492 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.483 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.458 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.748 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 107 | 112 | PF00244 | 0.373 |
LIG_BIR_III_2 | 177 | 181 | PF00653 | 0.487 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.456 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.670 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.383 |
LIG_LIR_Apic_2 | 46 | 52 | PF02991 | 0.459 |
LIG_NRBOX | 133 | 139 | PF00104 | 0.306 |
LIG_PTAP_UEV_1 | 411 | 416 | PF05743 | 0.612 |
LIG_PTB_Apo_2 | 205 | 212 | PF02174 | 0.447 |
LIG_PTB_Apo_2 | 340 | 347 | PF02174 | 0.501 |
LIG_PTB_Phospho_1 | 340 | 346 | PF10480 | 0.503 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.625 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.763 |
LIG_SH2_GRB2like | 369 | 372 | PF00017 | 0.526 |
LIG_SH2_GRB2like | 383 | 386 | PF00017 | 0.543 |
LIG_SH2_NCK_1 | 355 | 359 | PF00017 | 0.618 |
LIG_SH2_SRC | 369 | 372 | PF00017 | 0.516 |
LIG_SH2_SRC | 410 | 413 | PF00017 | 0.620 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.429 |
LIG_SH2_STAT3 | 345 | 348 | PF00017 | 0.637 |
LIG_SH2_STAT3 | 391 | 394 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.519 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.628 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.618 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.654 |
LIG_SUMO_SIM_anti_2 | 119 | 124 | PF11976 | 0.361 |
LIG_SUMO_SIM_anti_2 | 287 | 293 | PF11976 | 0.639 |
LIG_SUMO_SIM_par_1 | 166 | 172 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 191 | 198 | PF11976 | 0.623 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.401 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.500 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.655 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.544 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.471 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.678 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.532 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.361 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.495 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.654 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.377 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.694 |
MOD_DYRK1A_RPxSP_1 | 32 | 36 | PF00069 | 0.614 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.561 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.539 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.598 |
MOD_GlcNHglycan | 200 | 204 | PF01048 | 0.366 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.621 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.641 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.597 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.629 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.558 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.717 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.627 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.551 |
MOD_GlcNHglycan | 87 | 91 | PF01048 | 0.357 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.820 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.513 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.515 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.529 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.541 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.510 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.545 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.569 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.628 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.616 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.427 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.513 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.576 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.647 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.484 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.626 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.374 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.560 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.400 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.631 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.789 |
MOD_PK_1 | 116 | 122 | PF00069 | 0.361 |
MOD_PKA_1 | 116 | 122 | PF00069 | 0.494 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.432 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.424 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.444 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.447 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.384 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.671 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.606 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.553 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.630 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.788 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.707 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.653 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 163 | 168 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.452 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.607 |
TRG_NES_CRM1_1 | 92 | 106 | PF08389 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 109 | 113 | PF00026 | 0.560 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2V9 | Leptomonas seymouri | 33% | 100% |
A0A3Q8ICF2 | Leishmania donovani | 85% | 100% |
A4HE12 | Leishmania braziliensis | 55% | 99% |
A4I1B9 | Leishmania infantum | 85% | 100% |
Q4QA17 | Leishmania major | 83% | 100% |