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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: Q4QHW4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008233 | peptidase activity | 3 | 12 |
GO:0008236 | serine-type peptidase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017171 | serine hydrolase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.429 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.553 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.367 |
DEG_SPOP_SBC_1 | 325 | 329 | PF00917 | 0.443 |
DOC_CKS1_1 | 264 | 269 | PF01111 | 0.602 |
DOC_CKS1_1 | 34 | 39 | PF01111 | 0.557 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.433 |
DOC_MAPK_DCC_7 | 68 | 77 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 163 | 171 | PF00069 | 0.457 |
DOC_MAPK_RevD_3 | 277 | 293 | PF00069 | 0.407 |
DOC_PP2B_PxIxI_1 | 276 | 282 | PF00149 | 0.329 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.422 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.546 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 68 | 73 | PF00244 | 0.462 |
LIG_AP2alpha_2 | 314 | 316 | PF02296 | 0.430 |
LIG_APCC_ABBA_1 | 206 | 211 | PF00400 | 0.448 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.379 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.515 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.531 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.533 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.468 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.404 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.538 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.566 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.536 |
LIG_LIR_Apic_2 | 156 | 160 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 19 | 24 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 221 | 232 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 240 | 247 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 314 | 322 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.428 |
LIG_NRBOX | 118 | 124 | PF00104 | 0.539 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.453 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 52 | 56 | PF00017 | 0.480 |
LIG_SH2_PTP2 | 193 | 196 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.445 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.645 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.467 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.557 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.483 |
LIG_SUMO_SIM_anti_2 | 98 | 103 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 22 | 28 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 98 | 103 | PF11976 | 0.448 |
LIG_TRAF2_2 | 74 | 79 | PF00917 | 0.491 |
LIG_UBA3_1 | 244 | 248 | PF00899 | 0.491 |
LIG_UBA3_1 | 30 | 38 | PF00899 | 0.507 |
MOD_CDK_SPK_2 | 33 | 38 | PF00069 | 0.539 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.480 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.629 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.529 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.491 |
MOD_DYRK1A_RPxSP_1 | 263 | 267 | PF00069 | 0.452 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.528 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.252 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.259 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.257 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.372 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.246 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.380 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.596 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.451 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.465 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.513 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.501 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.570 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.503 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.570 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.573 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.486 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.519 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.561 |
MOD_N-GLC_1 | 85 | 90 | PF02516 | 0.205 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.374 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.551 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.510 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.582 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.465 |
MOD_NEK2_2 | 104 | 109 | PF00069 | 0.448 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.504 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.547 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.491 |
MOD_Plk_2-3 | 23 | 29 | PF00069 | 0.417 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.444 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.539 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.559 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.643 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.527 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.531 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.542 |
TRG_DiLeu_BaEn_1 | 60 | 65 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 194 | 197 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I426 | Leptomonas seymouri | 72% | 100% |
A0A0S4KJ65 | Bodo saltans | 39% | 93% |
A0A1X0NMP2 | Trypanosomatidae | 47% | 99% |
A0A3S7WQM7 | Leishmania donovani | 96% | 100% |
A0A422NV72 | Trypanosoma rangeli | 49% | 99% |
A4H5P2 | Leishmania braziliensis | 84% | 99% |
A4HTY1 | Leishmania infantum | 96% | 100% |
D0A9D7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AMR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
P41179 | Trypanosoma brucei brucei | 33% | 100% |
V5BII1 | Trypanosoma cruzi | 48% | 95% |