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 |
Related structures:
AlphaFold database: A4HFB3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0016485 | protein processing | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0051604 | protein maturation | 4 | 10 |
GO:0071586 | CAAX-box protein processing | 6 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004175 | endopeptidase activity | 4 | 10 |
GO:0004222 | metalloendopeptidase activity | 5 | 10 |
GO:0008233 | peptidase activity | 3 | 10 |
GO:0008237 | metallopeptidase activity | 4 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.201 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.180 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.233 |
CLV_PCSK_FUR_1 | 22 | 26 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.201 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.276 |
DEG_APCC_DBOX_1 | 139 | 147 | PF00400 | 0.461 |
DEG_APCC_DBOX_1 | 92 | 100 | PF00400 | 0.220 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.224 |
DOC_CYCLIN_RxL_1 | 89 | 98 | PF00134 | 0.201 |
DOC_MAPK_gen_1 | 149 | 156 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 54 | 62 | PF00069 | 0.405 |
DOC_MAPK_HePTP_8 | 146 | 158 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 149 | 158 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 54 | 62 | PF00069 | 0.461 |
DOC_MAPK_NFAT4_5 | 55 | 63 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 138 | 145 | PF00149 | 0.563 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.396 |
DOC_PP4_FxxP_1 | 115 | 118 | PF00568 | 0.607 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.335 |
LIG_14-3-3_CanoR_1 | 149 | 158 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 24 | 34 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 47 | 53 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 83 | 88 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.328 |
LIG_Actin_RPEL_3 | 143 | 162 | PF02755 | 0.405 |
LIG_Actin_WH2_2 | 239 | 257 | PF00022 | 0.278 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.348 |
LIG_BRCT_BRCA1_1 | 9 | 13 | PF00533 | 0.304 |
LIG_CtBP_PxDLS_1 | 248 | 252 | PF00389 | 0.457 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.304 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.251 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.208 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.503 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.387 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.317 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.609 |
LIG_LIR_Apic_2 | 114 | 118 | PF02991 | 0.609 |
LIG_LIR_Apic_2 | 15 | 21 | PF02991 | 0.253 |
LIG_LIR_Apic_2 | 85 | 90 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 257 | 266 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 59 | 70 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.349 |
LIG_NRBOX | 142 | 148 | PF00104 | 0.488 |
LIG_NRBOX | 215 | 221 | PF00104 | 0.396 |
LIG_NRBOX | 95 | 101 | PF00104 | 0.220 |
LIG_Pex14_2 | 13 | 17 | PF04695 | 0.250 |
LIG_Pex14_2 | 213 | 217 | PF04695 | 0.353 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.563 |
LIG_SH2_PTP2 | 18 | 21 | PF00017 | 0.284 |
LIG_SH2_SRC | 225 | 228 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.353 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.520 |
LIG_SUMO_SIM_anti_2 | 250 | 255 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 170 | 177 | PF11976 | 0.401 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.563 |
LIG_WRC_WIRS_1 | 112 | 117 | PF05994 | 0.554 |
LIG_WRC_WIRS_1 | 14 | 19 | PF05994 | 0.250 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.533 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.545 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.571 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.405 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.469 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.556 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.353 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.335 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.399 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.331 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.384 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.263 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.420 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.544 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.479 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.425 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.335 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.286 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.318 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.495 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.482 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.547 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.520 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.289 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.257 |
MOD_NEK2_2 | 266 | 271 | PF00069 | 0.220 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.459 |
MOD_PKA_1 | 149 | 155 | PF00069 | 0.457 |
MOD_PKA_1 | 54 | 60 | PF00069 | 0.461 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.506 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.459 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.478 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.456 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.465 |
MOD_PKB_1 | 54 | 62 | PF00069 | 0.405 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.566 |
MOD_Plk_2-3 | 46 | 52 | PF00069 | 0.517 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.269 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.224 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.239 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.624 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.393 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.489 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.477 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.273 |
MOD_SUMO_rev_2 | 183 | 192 | PF00179 | 0.501 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYS3 | Leptomonas seymouri | 50% | 100% |
A0A0S4JSY4 | Bodo saltans | 31% | 91% |
A0A1X0NYX6 | Trypanosomatidae | 31% | 94% |
A0A3S7X0B2 | Leishmania donovani | 75% | 100% |
A4I2J5 | Leishmania infantum | 75% | 100% |
C9ZK27 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 94% |
E9AYQ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q8S2 | Leishmania major | 70% | 100% |