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: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B1N0
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005509 | calcium ion binding | 5 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.214 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.264 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.244 |
CLV_PCSK_PC7_1 | 34 | 40 | PF00082 | 0.204 |
DOC_CYCLIN_yCln2_LP_2 | 184 | 190 | PF00134 | 0.432 |
DOC_PIKK_1 | 76 | 84 | PF02985 | 0.298 |
DOC_PP2B_LxvP_1 | 184 | 187 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 224 | 227 | PF13499 | 0.506 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.454 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.506 |
DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.307 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 38 | 46 | PF00244 | 0.253 |
LIG_14-3-3_CanoR_1 | 97 | 107 | PF00244 | 0.273 |
LIG_Actin_WH2_2 | 92 | 110 | PF00022 | 0.254 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.533 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.304 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.434 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.491 |
LIG_LIR_Apic_2 | 174 | 178 | PF02991 | 0.493 |
LIG_LIR_Apic_2 | 256 | 261 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 101 | 112 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 165 | 175 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.517 |
LIG_MAD2 | 44 | 52 | PF02301 | 0.227 |
LIG_MYND_1 | 227 | 231 | PF01753 | 0.420 |
LIG_PDZ_Class_1 | 269 | 274 | PF00595 | 0.483 |
LIG_PTB_Apo_2 | 169 | 176 | PF02174 | 0.467 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.637 |
LIG_SH2_SRC | 235 | 238 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.204 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.325 |
LIG_SH2_STAT3 | 200 | 203 | PF00017 | 0.527 |
LIG_SH2_STAT3 | 206 | 209 | PF00017 | 0.552 |
LIG_SH2_STAT3 | 213 | 216 | PF00017 | 0.582 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.310 |
LIG_SH3_1 | 211 | 217 | PF00018 | 0.452 |
LIG_SH3_1 | 258 | 264 | PF00018 | 0.534 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.613 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.539 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.551 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.524 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.609 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.630 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.675 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.204 |
LIG_SUMO_SIM_par_1 | 120 | 125 | PF11976 | 0.404 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.387 |
LIG_TRFH_1 | 213 | 217 | PF08558 | 0.453 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.204 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.470 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.393 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.342 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.509 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.481 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.505 |
MOD_PKA_1 | 34 | 40 | PF00069 | 0.260 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.447 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.453 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.567 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.595 |
MOD_SUMO_rev_2 | 139 | 146 | PF00179 | 0.345 |
TRG_DiLeu_BaLyEn_6 | 191 | 196 | PF01217 | 0.478 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.540 |
TRG_NLS_Bipartite_1 | 18 | 39 | PF00514 | 0.204 |
TRG_NLS_MonoExtC_3 | 34 | 39 | PF00514 | 0.204 |
TRG_NLS_MonoExtN_4 | 34 | 39 | PF00514 | 0.204 |
TRG_Pf-PMV_PEXEL_1 | 12 | 16 | PF00026 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.393 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3D0 | Leptomonas seymouri | 62% | 95% |
A0A3Q8IFD2 | Leishmania donovani | 33% | 98% |
A0A3S7X485 | Leishmania donovani | 44% | 100% |
A0A3S7X4C0 | Leishmania donovani | 68% | 100% |
A4HJ46 | Leishmania braziliensis | 38% | 96% |
A4HJ57 | Leishmania braziliensis | 60% | 87% |
A4HJ58 | Leishmania braziliensis | 53% | 100% |
A4I6G2 | Leishmania infantum | 33% | 98% |
A4I6H2 | Leishmania infantum | 68% | 100% |
A4I6H3 | Leishmania infantum | 45% | 100% |
E9B1L9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 98% |
Q9BHE7 | Leishmania major | 78% | 100% |
Q9BHE8 | Leishmania major | 45% | 99% |
Q9BHF8 | Leishmania major | 35% | 100% |