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: 26 |
NetGPI | no | yes: 0, no: 26 |
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: Q4QAJ3
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 | 26 |
GO:0005509 | calcium ion binding | 5 | 21 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 3 |
GO:0043167 | ion binding | 2 | 26 |
GO:0043169 | cation binding | 3 | 26 |
GO:0046872 | metal ion binding | 4 | 26 |
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 | 339 | 343 | PF00656 | 0.449 |
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.310 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.581 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.560 |
DOC_CYCLIN_RxL_1 | 271 | 281 | PF00134 | 0.422 |
DOC_MAPK_gen_1 | 286 | 294 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 62 | 71 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 272 | 279 | PF00149 | 0.443 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.574 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.660 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.562 |
LIG_APCC_ABBA_1 | 252 | 257 | PF00400 | 0.448 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.606 |
LIG_CaM_IQ_9 | 68 | 83 | PF13499 | 0.326 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.465 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.501 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.473 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.509 |
LIG_LIR_Apic_2 | 21 | 26 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 244 | 254 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 325 | 334 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 349 | 357 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 385 | 391 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.371 |
LIG_LYPXL_yS_3 | 150 | 153 | PF13949 | 0.505 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.437 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.550 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.258 |
LIG_SH2_GRB2like | 200 | 203 | PF00017 | 0.547 |
LIG_SH2_NCK_1 | 311 | 315 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.697 |
LIG_SH2_STAT3 | 200 | 203 | PF00017 | 0.775 |
LIG_SH2_STAT3 | 211 | 214 | PF00017 | 0.663 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.574 |
LIG_SH3_4 | 313 | 320 | PF00018 | 0.577 |
LIG_SUMO_SIM_anti_2 | 25 | 31 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 378 | 385 | PF11976 | 0.362 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.818 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.708 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.789 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.567 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.575 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.410 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.452 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.764 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.710 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.649 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.593 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.523 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.808 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.495 |
MOD_GlcNHglycan | 295 | 299 | PF01048 | 0.468 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.599 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.768 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.709 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.756 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.747 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.428 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.479 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.416 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.722 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.436 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.490 |
MOD_N-GLC_2 | 3 | 5 | PF02516 | 0.383 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.580 |
MOD_NEK2_2 | 379 | 384 | PF00069 | 0.417 |
MOD_OFUCOSY | 92 | 97 | PF10250 | 0.422 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.776 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.811 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.657 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.606 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.460 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.467 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.445 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.412 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.420 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.519 |
MOD_Plk_2-3 | 8 | 14 | PF00069 | 0.410 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.447 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.393 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.324 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.709 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.595 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.729 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.558 |
TRG_DiLeu_BaEn_1 | 349 | 354 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.436 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P229 | Leptomonas seymouri | 59% | 100% |
A0A0N1ILD7 | Leptomonas seymouri | 22% | 87% |
A0A0S4JBP2 | Bodo saltans | 24% | 88% |
A0A1X0NCU6 | Trypanosomatidae | 33% | 100% |
A0A3Q8IMS6 | Leishmania donovani | 95% | 100% |
A0A3R7KFH5 | Trypanosoma rangeli | 28% | 86% |
A0A3S5H5B1 | Leishmania donovani | 29% | 67% |
A0A3S7WWY0 | Leishmania donovani | 24% | 88% |
A0A3S7WYG1 | Leishmania donovani | 68% | 100% |
A4HDK3 | Leishmania braziliensis | 73% | 100% |
A4HDK4 | Leishmania braziliensis | 73% | 100% |
A4HS49 | Leishmania infantum | 29% | 67% |
A4HZP7 | Leishmania infantum | 24% | 88% |
A4I0X7 | Leishmania infantum | 94% | 100% |
A4I0X8 | Leishmania infantum | 67% | 100% |
C9ZWH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AK36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 67% |
E9AVK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 88% |
E9AWY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AWY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
O97201 | Leishmania major | 32% | 67% |
Q4QAJ2 | Leishmania major | 71% | 85% |
Q4QBX6 | Leishmania major | 25% | 88% |
V5B9E6 | Trypanosoma cruzi | 24% | 100% |
V5BK04 | Trypanosoma cruzi | 34% | 100% |