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: Q4QHP4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0016579 | protein deubiquitination | 6 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0036211 | protein modification process | 4 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043412 | macromolecule modification | 4 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0070646 | protein modification by small protein removal | 5 | 3 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 18 |
GO:0008233 | peptidase activity | 3 | 18 |
GO:0016787 | hydrolase activity | 2 | 18 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 3 |
GO:0101005 | deubiquitinase activity | 5 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 7 | 11 | PF00656 | 0.634 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.633 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.598 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.459 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 148 | 151 | PF00134 | 0.502 |
DOC_MAPK_MEF2A_6 | 169 | 177 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 181 | 188 | PF00069 | 0.442 |
DOC_PP1_RVXF_1 | 120 | 126 | PF00149 | 0.405 |
DOC_PP1_RVXF_1 | 20 | 27 | PF00149 | 0.429 |
DOC_PP2B_LxvP_1 | 148 | 151 | PF13499 | 0.503 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.557 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 240 | 244 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 47 | 53 | PF00244 | 0.514 |
LIG_14-3-3_CterR_2 | 251 | 254 | PF00244 | 0.510 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.583 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.553 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.509 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.468 |
LIG_LIR_LC3C_4 | 113 | 117 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.429 |
LIG_MLH1_MIPbox_1 | 215 | 219 | PF16413 | 0.393 |
LIG_MYND_1 | 185 | 189 | PF01753 | 0.375 |
LIG_Pex14_2 | 140 | 144 | PF04695 | 0.429 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.434 |
LIG_SH2_SRC | 72 | 75 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.536 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.356 |
LIG_SUMO_SIM_par_1 | 171 | 176 | PF11976 | 0.435 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.502 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.482 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.586 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.509 |
MOD_DYRK1A_RPxSP_1 | 240 | 244 | PF00069 | 0.554 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.353 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.622 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.675 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.534 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.727 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.510 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.463 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.772 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.419 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.332 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.589 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.482 |
MOD_NEK2_2 | 82 | 87 | PF00069 | 0.405 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.496 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.640 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.369 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.604 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.532 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.713 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.372 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.600 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.567 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.522 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.792 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.452 |
TRG_DiLeu_BaEn_1 | 111 | 116 | PF01217 | 0.509 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVE7 | Leptomonas seymouri | 55% | 100% |
A0A0N1PCI8 | Leptomonas seymouri | 55% | 100% |
A0A0S4JCD5 | Bodo saltans | 25% | 93% |
A0A1X0NHT4 | Trypanosomatidae | 40% | 88% |
A0A3Q8IAW2 | Leishmania donovani | 59% | 100% |
A0A3S7WQX3 | Leishmania donovani | 93% | 100% |
A0A422NZN2 | Trypanosoma rangeli | 41% | 100% |
A4H5V8 | Leishmania braziliensis | 56% | 100% |
A4HU52 | Leishmania infantum | 59% | 100% |
A4HU53 | Leishmania infantum | 93% | 100% |
D0A9M8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 76% |
D0A9N3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AMY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9AMY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QHP5 | Leishmania major | 60% | 100% |
V5BMK8 | Trypanosoma cruzi | 41% | 77% |