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: Q4QFL0
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 4 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016043 | cellular component organization | 3 | 4 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 4 |
GO:0003677 | DNA binding | 4 | 4 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0005488 | binding | 1 | 4 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.579 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.421 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.267 |
DEG_COP1_1 | 276 | 285 | PF00400 | 0.500 |
DEG_SCF_FBW7_1 | 267 | 273 | PF00400 | 0.487 |
DOC_CKS1_1 | 267 | 272 | PF01111 | 0.484 |
DOC_MAPK_MEF2A_6 | 95 | 103 | PF00069 | 0.507 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.489 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.728 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 216 | 220 | PF00244 | 0.467 |
LIG_Actin_WH2_2 | 75 | 93 | PF00022 | 0.471 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.627 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.416 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.503 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.370 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.599 |
LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.450 |
LIG_PTAP_UEV_1 | 282 | 287 | PF05743 | 0.509 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.416 |
LIG_SH3_1 | 145 | 151 | PF00018 | 0.616 |
LIG_SH3_1 | 159 | 165 | PF00018 | 0.609 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.761 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.676 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.593 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.547 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.619 |
LIG_TRAF2_1 | 218 | 221 | PF00917 | 0.507 |
MOD_CDC14_SPxK_1 | 141 | 144 | PF00782 | 0.695 |
MOD_CDK_SPxK_1 | 138 | 144 | PF00069 | 0.664 |
MOD_CDK_SPxxK_3 | 138 | 145 | PF00069 | 0.653 |
MOD_CDK_SPxxK_3 | 200 | 207 | PF00069 | 0.480 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.562 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.657 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.514 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.623 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.454 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.635 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.584 |
MOD_Cter_Amidation | 57 | 60 | PF01082 | 0.533 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.659 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.652 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.552 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.783 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.590 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.617 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.669 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.429 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.479 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.561 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.654 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.672 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.493 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.449 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.618 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.521 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.609 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.614 |
MOD_SUMO_rev_2 | 152 | 160 | PF00179 | 0.762 |
TRG_DiLeu_BaEn_4 | 220 | 226 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.521 |
TRG_NLS_Bipartite_1 | 144 | 162 | PF00514 | 0.689 |
TRG_NLS_MonoExtC_3 | 157 | 162 | PF00514 | 0.652 |
TRG_Pf-PMV_PEXEL_1 | 246 | 250 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2C3 | Leptomonas seymouri | 60% | 88% |
A0A3Q8IC32 | Leishmania donovani | 95% | 100% |
A0A422MT09 | Trypanosoma rangeli | 44% | 81% |
A4H7U4 | Leishmania braziliensis | 78% | 100% |
A4HW70 | Leishmania infantum | 95% | 100% |
C9ZSU9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 99% |
E9APX1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 98% |
V5AW13 | Trypanosoma cruzi | 40% | 83% |