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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HDS5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016874 | ligase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.567 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.367 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.367 |
CLV_PCSK_PC7_1 | 254 | 260 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.618 |
DEG_APCC_DBOX_1 | 311 | 319 | PF00400 | 0.532 |
DEG_SCF_FBW7_1 | 81 | 88 | PF00400 | 0.426 |
DEG_SPOP_SBC_1 | 111 | 115 | PF00917 | 0.221 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.463 |
DEG_SPOP_SBC_1 | 61 | 65 | PF00917 | 0.484 |
DOC_CYCLIN_RxL_1 | 16 | 28 | PF00134 | 0.376 |
DOC_CYCLIN_yCln2_LP_2 | 71 | 74 | PF00134 | 0.375 |
DOC_MAPK_DCC_7 | 132 | 142 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 189 | 195 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 26 | 32 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 206 | 214 | PF00069 | 0.443 |
DOC_PP2B_LxvP_1 | 171 | 174 | PF13499 | 0.480 |
DOC_PP2B_LxvP_1 | 70 | 73 | PF13499 | 0.387 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.310 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.300 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 110 | 118 | PF00244 | 0.252 |
LIG_14-3-3_CanoR_1 | 206 | 210 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 231 | 236 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 258 | 268 | PF00244 | 0.467 |
LIG_AP_GAE_1 | 90 | 96 | PF02883 | 0.433 |
LIG_APCC_ABBA_1 | 192 | 197 | PF00400 | 0.348 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.613 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.495 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 225 | 230 | PF00928 | 0.449 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.315 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.477 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.592 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.469 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.476 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.515 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.547 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.513 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.608 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.496 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.362 |
LIG_LIR_Gen_1 | 196 | 207 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 281 | 289 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.458 |
LIG_Pex14_2 | 125 | 129 | PF04695 | 0.363 |
LIG_Pex14_2 | 283 | 287 | PF04695 | 0.578 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.580 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.264 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.352 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.441 |
LIG_SH3_4 | 269 | 276 | PF00018 | 0.529 |
LIG_SUMO_SIM_anti_2 | 264 | 269 | PF11976 | 0.559 |
LIG_SUMO_SIM_anti_2 | 68 | 73 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.487 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.466 |
LIG_WW_1 | 73 | 76 | PF00397 | 0.526 |
MOD_CDK_SPxxK_3 | 113 | 120 | PF00069 | 0.300 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.341 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.532 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.708 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.466 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.661 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.628 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.527 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.512 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.568 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.467 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.701 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.508 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.680 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.715 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.404 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.724 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.615 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.609 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.686 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.690 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.726 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.533 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.494 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.737 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.638 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.308 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.344 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.380 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.461 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.305 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.342 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.440 |
MOD_PKB_1 | 110 | 118 | PF00069 | 0.199 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.408 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.454 |
MOD_Plk_2-3 | 300 | 306 | PF00069 | 0.757 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.342 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.305 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.718 |
TRG_AP2beta_CARGO_1 | 17 | 27 | PF09066 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 147 | 152 | PF01217 | 0.225 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.199 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.317 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.358 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3S2 | Leptomonas seymouri | 48% | 100% |
A0A1X0NWL0 | Trypanosomatidae | 32% | 100% |
A0A3Q8ID23 | Leishmania donovani | 72% | 98% |
A0A3S5IS47 | Trypanosoma rangeli | 35% | 100% |
A4I123 | Leishmania infantum | 72% | 98% |
E9AX60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 98% |
Q4QAB6 | Leishmania major | 73% | 100% |
V5BEA3 | Trypanosoma cruzi | 34% | 99% |