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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AMY2
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016579 | protein deubiquitination | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070646 | protein modification by small protein removal | 5 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 18 |
GO:0008233 | peptidase activity | 3 | 18 |
GO:0016787 | hydrolase activity | 2 | 18 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 18 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 2 |
GO:0101005 | deubiquitinase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.454 |
CLV_C14_Caspase3-7 | 7 | 11 | PF00656 | 0.703 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.670 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.617 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.571 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.625 |
DOC_CYCLIN_yCln2_LP_2 | 148 | 151 | PF00134 | 0.542 |
DOC_MAPK_MEF2A_6 | 169 | 177 | PF00069 | 0.608 |
DOC_MAPK_MEF2A_6 | 181 | 188 | PF00069 | 0.499 |
DOC_PP1_RVXF_1 | 120 | 126 | PF00149 | 0.454 |
DOC_PP2B_LxvP_1 | 148 | 151 | PF13499 | 0.542 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.559 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 240 | 244 | PF00244 | 0.618 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.606 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.608 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.523 |
LIG_LIR_LC3C_4 | 113 | 117 | PF02991 | 0.454 |
LIG_MLH1_MIPbox_1 | 215 | 219 | PF16413 | 0.460 |
LIG_MYND_1 | 185 | 189 | PF01753 | 0.442 |
LIG_PCNA_yPIPBox_3 | 31 | 44 | PF02747 | 0.358 |
LIG_PDZ_Class_1 | 249 | 254 | PF00595 | 0.498 |
LIG_Pex14_2 | 140 | 144 | PF04695 | 0.468 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.473 |
LIG_SH2_SRC | 72 | 75 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.646 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.559 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.586 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.420 |
LIG_SUMO_SIM_par_1 | 171 | 176 | PF11976 | 0.487 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.484 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.557 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.464 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.631 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.512 |
MOD_DYRK1A_RPxSP_1 | 240 | 244 | PF00069 | 0.618 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.369 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.720 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.590 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.543 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.504 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.778 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.442 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.402 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.619 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.479 |
MOD_NEK2_2 | 204 | 209 | PF00069 | 0.408 |
MOD_NEK2_2 | 82 | 87 | PF00069 | 0.454 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.486 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.631 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.421 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.416 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.575 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.562 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.742 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.636 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.613 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.524 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.794 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.493 |
TRG_DiLeu_BaEn_1 | 111 | 116 | PF01217 | 0.537 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 159 | 161 | PF00400 | 0.347 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVE7 | Leptomonas seymouri | 54% | 100% |
A0A0N1PCI8 | Leptomonas seymouri | 53% | 100% |
A0A0S4JCD5 | Bodo saltans | 25% | 93% |
A0A1X0NHT4 | Trypanosomatidae | 38% | 88% |
A0A3Q8IAW2 | Leishmania donovani | 57% | 100% |
A0A3S7WQX3 | Leishmania donovani | 91% | 100% |
A0A422NZN2 | Trypanosoma rangeli | 39% | 100% |
A4H5V8 | Leishmania braziliensis | 57% | 100% |
A4HU52 | Leishmania infantum | 57% | 100% |
A4HU53 | Leishmania infantum | 91% | 100% |
D0A9M8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 76% |
D0A9N3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AMY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
Q4QHP4 | Leishmania major | 89% | 100% |
Q4QHP5 | Leishmania major | 57% | 100% |
V5BMK8 | Trypanosoma cruzi | 41% | 77% |