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: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 16 |
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AR51
Term | Name | Level | Count |
---|---|---|---|
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0009308 | amine metabolic process | 4 | 9 |
GO:0009690 | cytokinin metabolic process | 3 | 9 |
GO:0009691 | cytokinin biosynthetic process | 4 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0010817 | regulation of hormone levels | 3 | 9 |
GO:0042445 | hormone metabolic process | 2 | 9 |
GO:0042446 | hormone biosynthetic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044249 | cellular biosynthetic process | 3 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0065007 | biological regulation | 1 | 9 |
GO:0065008 | regulation of biological quality | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 1 |
GO:0016799 | hydrolase activity, hydrolyzing N-glycosyl compounds | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.272 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.367 |
DOC_MAPK_gen_1 | 254 | 262 | PF00069 | 0.476 |
DOC_PP1_RVXF_1 | 216 | 223 | PF00149 | 0.472 |
DOC_PP2B_PxIxI_1 | 254 | 260 | PF00149 | 0.523 |
DOC_PP4_FxxP_1 | 265 | 268 | PF00568 | 0.470 |
DOC_PP4_FxxP_1 | 306 | 309 | PF00568 | 0.386 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.340 |
DOC_USP7_UBL2_3 | 148 | 152 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 207 | 214 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 62 | 67 | PF00244 | 0.558 |
LIG_AP2alpha_1 | 20 | 24 | PF02296 | 0.539 |
LIG_AP2alpha_1 | 265 | 269 | PF02296 | 0.480 |
LIG_AP2alpha_2 | 267 | 269 | PF02296 | 0.470 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.478 |
LIG_EVH1_2 | 309 | 313 | PF00568 | 0.309 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.384 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.512 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.496 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.482 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.472 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.472 |
LIG_GSK3_LRP6_1 | 308 | 314 | PF00069 | 0.492 |
LIG_LIR_Apic_2 | 263 | 268 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 305 | 309 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 237 | 245 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 267 | 277 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 284 | 294 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 311 | 317 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 61 | 69 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.666 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 237 | 241 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.544 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.496 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.473 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.558 |
LIG_SH2_NCK_1 | 209 | 213 | PF00017 | 0.523 |
LIG_SH2_NCK_1 | 99 | 103 | PF00017 | 0.558 |
LIG_SH2_SRC | 28 | 31 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 99 | 103 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.498 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.465 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.495 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.472 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 239 | 246 | PF11976 | 0.474 |
LIG_SUMO_SIM_anti_2 | 295 | 301 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 239 | 246 | PF11976 | 0.472 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.538 |
LIG_TYR_ITIM | 55 | 60 | PF00017 | 0.491 |
LIG_TYR_ITSM | 95 | 102 | PF00017 | 0.526 |
LIG_UBA3_1 | 171 | 177 | PF00899 | 0.203 |
LIG_WRC_WIRS_1 | 235 | 240 | PF05994 | 0.496 |
LIG_WRC_WIRS_1 | 303 | 308 | PF05994 | 0.455 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.568 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.519 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.593 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.393 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.472 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.472 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.545 |
MOD_GlcNHglycan | 198 | 202 | PF01048 | 0.309 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.456 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.436 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.502 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.598 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.492 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.525 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.343 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.445 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.624 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.440 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.396 |
MOD_NEK2_2 | 5 | 10 | PF00069 | 0.526 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.651 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.458 |
MOD_PK_1 | 185 | 191 | PF00069 | 0.539 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.477 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.436 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.478 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.472 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.506 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.477 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.520 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.456 |
MOD_SUMO_rev_2 | 13 | 21 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 156 | 161 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 215 | 220 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 279 | 287 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 92 | 97 | PF00179 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 120 | 125 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.643 |
TRG_Pf-PMV_PEXEL_1 | 274 | 279 | PF00026 | 0.323 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC81 | Leptomonas seymouri | 69% | 100% |
A0A1X0NSV2 | Trypanosomatidae | 47% | 94% |
A0A3Q8IDZ9 | Leishmania donovani | 93% | 100% |
A0A422MP54 | Trypanosoma rangeli | 51% | 100% |
A4H924 | Leishmania braziliensis | 83% | 100% |
A4HXF6 | Leishmania infantum | 93% | 100% |
K3VH30 | Fusarium pseudograminearum (strain CS3096) | 33% | 66% |
P47044 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
Q4QEB2 | Leishmania major | 92% | 100% |