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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4Q2H1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 122 | 128 | PF00089 | 0.676 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.634 |
CLV_PCSK_FUR_1 | 292 | 296 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.563 |
CLV_PCSK_PC7_1 | 108 | 114 | PF00082 | 0.623 |
CLV_PCSK_PC7_1 | 262 | 268 | PF00082 | 0.681 |
CLV_PCSK_PC7_1 | 295 | 301 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.602 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.686 |
DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.586 |
DOC_ANK_TNKS_1 | 83 | 90 | PF00023 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 244 | 250 | PF00134 | 0.611 |
DOC_MAPK_gen_1 | 181 | 189 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 192 | 200 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 211 | 221 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 275 | 285 | PF00069 | 0.579 |
DOC_PP1_RVXF_1 | 117 | 124 | PF00149 | 0.573 |
DOC_PP1_RVXF_1 | 162 | 168 | PF00149 | 0.574 |
DOC_PP1_RVXF_1 | 216 | 222 | PF00149 | 0.677 |
DOC_PP1_RVXF_1 | 57 | 64 | PF00149 | 0.718 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.418 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 211 | 217 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 220 | 227 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 229 | 233 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 317 | 324 | PF00244 | 0.691 |
LIG_14-3-3_CterR_2 | 344 | 347 | PF00244 | 0.710 |
LIG_Actin_WH2_2 | 294 | 309 | PF00022 | 0.508 |
LIG_Actin_WH2_2 | 99 | 114 | PF00022 | 0.680 |
LIG_APCC_ABBAyCdc20_2 | 144 | 150 | PF00400 | 0.597 |
LIG_CaM_IQ_9 | 111 | 127 | PF13499 | 0.571 |
LIG_deltaCOP1_diTrp_1 | 168 | 173 | PF00928 | 0.662 |
LIG_deltaCOP1_diTrp_1 | 291 | 296 | PF00928 | 0.649 |
LIG_deltaCOP1_diTrp_1 | 95 | 101 | PF00928 | 0.621 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.647 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.644 |
LIG_LIR_Gen_1 | 241 | 250 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 332 | 336 | PF02991 | 0.615 |
LIG_Pex14_1 | 173 | 177 | PF04695 | 0.438 |
LIG_SH2_NCK_1 | 53 | 57 | PF00017 | 0.608 |
LIG_SH2_SRC | 53 | 56 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.674 |
LIG_SH2_STAT3 | 177 | 180 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.702 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.668 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.625 |
LIG_WRC_WIRS_1 | 12 | 17 | PF05994 | 0.553 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.721 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.716 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.703 |
MOD_CMANNOS | 167 | 170 | PF00535 | 0.595 |
MOD_CMANNOS | 293 | 296 | PF00535 | 0.547 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.598 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.743 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.761 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.604 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.665 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.597 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.580 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.549 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.825 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.619 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.552 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.570 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.599 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.691 |
TRG_DiLeu_BaEn_1 | 311 | 316 | PF01217 | 0.617 |
TRG_DiLeu_BaLyEn_6 | 272 | 277 | PF01217 | 0.630 |
TRG_DiLeu_BaLyEn_6 | 310 | 315 | PF01217 | 0.650 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.679 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 140 | 145 | PF00026 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 156 | 160 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILB8 | Leptomonas seymouri | 57% | 100% |
A0A1X0PA21 | Trypanosomatidae | 29% | 100% |
A0A3Q8IFU3 | Leishmania donovani | 89% | 100% |
A4HB92 | Leishmania braziliensis | 75% | 100% |
A4IAE0 | Leishmania infantum | 89% | 100% |
E9B5G4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |