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: A0A3Q8ID23
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 | 245 | 249 | PF00656 | 0.507 |
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.615 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.445 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.564 |
CLV_PCSK_PC7_1 | 254 | 260 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.522 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.578 |
DEG_ODPH_VHL_1 | 99 | 111 | PF01847 | 0.272 |
DEG_SCF_FBW7_2 | 41 | 46 | PF00400 | 0.602 |
DEG_SPOP_SBC_1 | 59 | 63 | PF00917 | 0.597 |
DOC_CYCLIN_RxL_1 | 16 | 28 | PF00134 | 0.452 |
DOC_CYCLIN_yCln2_LP_2 | 71 | 74 | PF00134 | 0.433 |
DOC_MAPK_DCC_7 | 132 | 142 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 197 | 203 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 26 | 32 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 214 | 222 | PF00069 | 0.504 |
DOC_PP1_RVXF_1 | 224 | 230 | PF00149 | 0.439 |
DOC_PP2B_LxvP_1 | 70 | 73 | PF13499 | 0.445 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.344 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.646 |
DOC_USP7_MATH_2 | 231 | 237 | PF00917 | 0.517 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 263 | 273 | PF00244 | 0.529 |
LIG_Actin_WH2_2 | 52 | 69 | PF00022 | 0.640 |
LIG_APCC_ABBA_1 | 200 | 205 | PF00400 | 0.419 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.635 |
LIG_deltaCOP1_diTrp_1 | 233 | 238 | PF00928 | 0.601 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.489 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.530 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.743 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.496 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.534 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.552 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.662 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.567 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.603 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.729 |
LIG_LIR_Apic_2 | 236 | 241 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.433 |
LIG_MYND_1 | 97 | 101 | PF01753 | 0.529 |
LIG_Pex14_2 | 125 | 129 | PF04695 | 0.423 |
LIG_Pex14_2 | 288 | 292 | PF04695 | 0.637 |
LIG_SH2_NCK_1 | 207 | 211 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.610 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.400 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.296 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.369 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.590 |
LIG_SH3_4 | 274 | 281 | PF00018 | 0.681 |
LIG_SUMO_SIM_anti_2 | 269 | 274 | PF11976 | 0.703 |
LIG_SUMO_SIM_anti_2 | 68 | 73 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 138 | 143 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.503 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.521 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.706 |
LIG_WW_1 | 73 | 76 | PF00397 | 0.568 |
MOD_CDC14_SPxK_1 | 182 | 185 | PF00782 | 0.714 |
MOD_CDC14_SPxK_1 | 64 | 67 | PF00782 | 0.414 |
MOD_CDK_SPxK_1 | 179 | 185 | PF00069 | 0.714 |
MOD_CDK_SPxK_1 | 61 | 67 | PF00069 | 0.455 |
MOD_CDK_SPxxK_3 | 113 | 120 | PF00069 | 0.369 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.485 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.560 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.758 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.677 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.621 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.761 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.741 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.473 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.671 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.730 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.689 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.677 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.665 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.649 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.728 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.740 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.533 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.668 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.602 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.747 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.781 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.676 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.665 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.452 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.427 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.445 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.585 |
MOD_NEK2_2 | 192 | 197 | PF00069 | 0.621 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.513 |
MOD_PK_1 | 51 | 57 | PF00069 | 0.725 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.426 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.569 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.498 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.426 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.324 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.735 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.731 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.487 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.684 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.706 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.561 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.721 |
TRG_AP2beta_CARGO_1 | 17 | 27 | PF09066 | 0.591 |
TRG_DiLeu_BaLyEn_6 | 223 | 228 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3S2 | Leptomonas seymouri | 51% | 100% |
A0A1X0NWL0 | Trypanosomatidae | 34% | 100% |
A0A3S5IS47 | Trypanosoma rangeli | 34% | 100% |
A4HDS5 | Leishmania braziliensis | 72% | 98% |
A4I123 | Leishmania infantum | 99% | 100% |
E9AX60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QAB6 | Leishmania major | 91% | 100% |
V5BEA3 | Trypanosoma cruzi | 34% | 100% |