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 | yes | yes: 4, no: 1 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4QFQ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.517 |
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.579 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.732 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.832 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.844 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.832 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.755 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.764 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.744 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.772 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.629 |
DEG_SPOP_SBC_1 | 159 | 163 | PF00917 | 0.608 |
DEG_SPOP_SBC_1 | 317 | 321 | PF00917 | 0.552 |
DOC_CKS1_1 | 124 | 129 | PF01111 | 0.472 |
DOC_MAPK_gen_1 | 351 | 359 | PF00069 | 0.575 |
DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.688 |
DOC_PP2B_PxIxI_1 | 284 | 290 | PF00149 | 0.599 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.530 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 150 | 160 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 224 | 229 | PF00244 | 0.508 |
LIG_APCC_ABBA_1 | 25 | 30 | PF00400 | 0.471 |
LIG_BRCT_BRCA1_1 | 385 | 389 | PF00533 | 0.491 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.474 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.517 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.636 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.557 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.378 |
LIG_PDZ_Class_2 | 391 | 396 | PF00595 | 0.530 |
LIG_Pex14_2 | 392 | 396 | PF04695 | 0.452 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.498 |
LIG_SH2_NCK_1 | 124 | 128 | PF00017 | 0.498 |
LIG_SH2_NCK_1 | 182 | 186 | PF00017 | 0.515 |
LIG_SH2_SRC | 182 | 185 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.568 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.585 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.517 |
LIG_SUMO_SIM_par_1 | 21 | 30 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 285 | 291 | PF11976 | 0.599 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.599 |
LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.524 |
MOD_CDK_SPK_2 | 108 | 113 | PF00069 | 0.720 |
MOD_CDK_SPK_2 | 184 | 189 | PF00069 | 0.592 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.795 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.687 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.740 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.738 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.775 |
MOD_Cter_Amidation | 82 | 85 | PF01082 | 0.759 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.706 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.595 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.733 |
MOD_GlcNHglycan | 237 | 241 | PF01048 | 0.816 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.747 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.778 |
MOD_GlcNHglycan | 371 | 375 | PF01048 | 0.711 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.726 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.769 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.712 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.722 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.745 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.734 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.728 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.365 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.553 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.530 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.714 |
MOD_NEK2_2 | 379 | 384 | PF00069 | 0.530 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.639 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.795 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.756 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.673 |
MOD_PKB_1 | 251 | 259 | PF00069 | 0.646 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.763 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.654 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.799 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.374 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.826 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.580 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.589 |
MOD_SUMO_rev_2 | 336 | 342 | PF00179 | 0.673 |
MOD_SUMO_rev_2 | 76 | 86 | PF00179 | 0.819 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.692 |
TRG_ER_diArg_1 | 250 | 253 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.710 |
TRG_NLS_Bipartite_1 | 148 | 169 | PF00514 | 0.775 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.621 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WT04 | Leishmania donovani | 86% | 100% |
A4H7N2 | Leishmania braziliensis | 55% | 98% |
A4HW21 | Leishmania infantum | 86% | 100% |
E9APS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 93% |