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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H5V8
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 | 16 |
GO:0008233 | peptidase activity | 3 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 16 |
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 | 213 | 217 | PF00656 | 0.418 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.504 |
DEG_APCC_DBOX_1 | 160 | 168 | PF00400 | 0.281 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.234 |
DOC_CYCLIN_yCln2_LP_2 | 150 | 153 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 188 | 191 | PF00134 | 0.372 |
DOC_MAPK_MEF2A_6 | 182 | 189 | PF00069 | 0.406 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.447 |
DOC_PP2B_LxvP_1 | 188 | 191 | PF13499 | 0.354 |
DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.474 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.465 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 91 | 95 | PF00244 | 0.491 |
LIG_APCC_ABBA_1 | 189 | 194 | PF00400 | 0.268 |
LIG_eIF4E_1 | 183 | 189 | PF01652 | 0.380 |
LIG_LIR_Apic_2 | 216 | 222 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.432 |
LIG_MYND_1 | 186 | 190 | PF01753 | 0.340 |
LIG_Pex14_2 | 142 | 146 | PF04695 | 0.422 |
LIG_Pex14_2 | 98 | 102 | PF04695 | 0.509 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.435 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.376 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.514 |
LIG_SH2_STAT3 | 103 | 106 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.541 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.339 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.403 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.367 |
LIG_WRC_WIRS_1 | 118 | 123 | PF05994 | 0.422 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.636 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.482 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.329 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.608 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.605 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.519 |
MOD_GlcNHglycan | 80 | 85 | PF01048 | 0.295 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.461 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.388 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.503 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.609 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.502 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.496 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.415 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.427 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.463 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.483 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.314 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.397 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.439 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.674 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.412 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.527 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.541 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.406 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.481 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.612 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.438 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVE7 | Leptomonas seymouri | 50% | 91% |
A0A0N1PCI8 | Leptomonas seymouri | 62% | 99% |
A0A0S4JCD5 | Bodo saltans | 25% | 81% |
A0A1X0NHT4 | Trypanosomatidae | 41% | 77% |
A0A3Q8IAW2 | Leishmania donovani | 76% | 100% |
A0A3S7WQX3 | Leishmania donovani | 59% | 87% |
A0A422NZN2 | Trypanosoma rangeli | 38% | 91% |
A4HU52 | Leishmania infantum | 76% | 100% |
A4HU53 | Leishmania infantum | 59% | 87% |
D0A9N3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 94% |
E9AMY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9AMY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 87% |
H2KZK4 | Caenorhabditis elegans | 27% | 66% |
Q4QHP4 | Leishmania major | 56% | 100% |
Q4QHP5 | Leishmania major | 75% | 98% |
Q93VG8 | Arabidopsis thaliana | 30% | 99% |
V5BMK8 | Trypanosoma cruzi | 42% | 67% |