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: 24 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0031974 | membrane-enclosed lumen | 2 | 3 |
GO:0031981 | nuclear lumen | 5 | 3 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 3 |
GO:0043233 | organelle lumen | 3 | 3 |
GO:0070013 | intracellular organelle lumen | 4 | 3 |
GO:0097014 | ciliary plasm | 5 | 3 |
GO:0099568 | cytoplasmic region | 3 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QAJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0016567 | protein ubiquitination | 7 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0032446 | protein modification by small protein conjugation | 6 | 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: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 | 3 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 3 |
GO:0005488 | binding | 1 | 24 |
GO:0005509 | calcium ion binding | 5 | 18 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 3 |
GO:0043167 | ion binding | 2 | 24 |
GO:0043169 | cation binding | 3 | 24 |
GO:0046872 | metal ion binding | 4 | 24 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 3 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 279 | 283 | PF00656 | 0.459 |
CLV_C14_Caspase3-7 | 299 | 303 | PF00656 | 0.334 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.579 |
DEG_SPOP_SBC_1 | 102 | 106 | PF00917 | 0.716 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.739 |
DOC_CYCLIN_RxL_1 | 211 | 221 | PF00134 | 0.476 |
DOC_MAPK_gen_1 | 226 | 234 | PF00069 | 0.617 |
DOC_MAPK_MEF2A_6 | 62 | 71 | PF00069 | 0.491 |
DOC_PP1_RVXF_1 | 212 | 219 | PF00149 | 0.468 |
DOC_PP4_MxPP_1 | 110 | 113 | PF00568 | 0.568 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.672 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.577 |
LIG_14-3-3_CanoR_1 | 127 | 137 | PF00244 | 0.453 |
LIG_APCC_ABBA_1 | 192 | 197 | PF00400 | 0.463 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.572 |
LIG_CaM_IQ_9 | 68 | 83 | PF13499 | 0.340 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.495 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.521 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.355 |
LIG_LIR_Apic_2 | 125 | 129 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 21 | 26 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 265 | 274 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 289 | 297 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.367 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.511 |
LIG_SH2_CRK | 140 | 144 | PF00017 | 0.491 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.433 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.569 |
LIG_SH2_CRK | 267 | 271 | PF00017 | 0.247 |
LIG_SH2_NCK_1 | 140 | 144 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 251 | 255 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.711 |
LIG_SH2_STAP1 | 186 | 190 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.635 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.685 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.761 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.737 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.597 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.579 |
LIG_SH3_4 | 253 | 260 | PF00018 | 0.602 |
LIG_SUMO_SIM_anti_2 | 25 | 31 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 318 | 325 | PF11976 | 0.418 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.728 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.456 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.431 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.717 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.744 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.756 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.531 |
MOD_GlcNHglycan | 235 | 239 | PF01048 | 0.465 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.584 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.581 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.624 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.719 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.472 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.512 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.429 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.469 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.510 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.698 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.573 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.384 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.490 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.502 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.385 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.450 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.418 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.530 |
MOD_Plk_2-3 | 8 | 14 | PF00069 | 0.434 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.462 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.427 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.345 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.741 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.629 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.574 |
TRG_DiLeu_BaEn_1 | 289 | 294 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P229 | Leptomonas seymouri | 53% | 100% |
A0A0N1ILD7 | Leptomonas seymouri | 23% | 74% |
A0A0S4JBP2 | Bodo saltans | 25% | 74% |
A0A1X0NCU6 | Trypanosomatidae | 49% | 100% |
A0A1X0NKY5 | Trypanosomatidae | 32% | 76% |
A0A1X0NTS2 | Trypanosomatidae | 26% | 75% |
A0A3Q8IMS6 | Leishmania donovani | 70% | 85% |
A0A3R7KFH5 | Trypanosoma rangeli | 45% | 73% |
A0A3S7WWY0 | Leishmania donovani | 27% | 75% |
A0A3S7WYG1 | Leishmania donovani | 95% | 100% |
A4HDK3 | Leishmania braziliensis | 59% | 85% |
A4HDK4 | Leishmania braziliensis | 59% | 85% |
A4HZP7 | Leishmania infantum | 27% | 75% |
A4I0X7 | Leishmania infantum | 70% | 85% |
A4I0X8 | Leishmania infantum | 94% | 100% |
C9ZWH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AVK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 75% |
E9AWY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 85% |
E9AWY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QAJ3 | Leishmania major | 71% | 85% |
Q4QBX6 | Leishmania major | 27% | 75% |
V5B9E6 | Trypanosoma cruzi | 33% | 87% |
V5BK04 | Trypanosoma cruzi | 48% | 100% |