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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AVK3
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 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: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:0005488 | binding | 1 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043169 | cation binding | 3 | 14 |
GO:0046872 | metal ion binding | 4 | 14 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
GO:0005509 | calcium ion binding | 5 | 8 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 2 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 2 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.483 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.366 |
CLV_PCSK_FUR_1 | 404 | 408 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 406 | 408 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.429 |
DOC_ANK_TNKS_1 | 38 | 45 | PF00023 | 0.362 |
DOC_CKS1_1 | 58 | 63 | PF01111 | 0.439 |
DOC_CYCLIN_yCln2_LP_2 | 144 | 150 | PF00134 | 0.561 |
DOC_MAPK_FxFP_2 | 237 | 240 | PF00069 | 0.232 |
DOC_PP1_RVXF_1 | 230 | 237 | PF00149 | 0.458 |
DOC_PP4_FxxP_1 | 237 | 240 | PF00568 | 0.232 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.561 |
DOC_USP7_MATH_2 | 156 | 162 | PF00917 | 0.502 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.301 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.431 |
LIG_14-3-3_CanoR_1 | 185 | 189 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.401 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.524 |
LIG_BRCT_BRCA1_1 | 260 | 264 | PF00533 | 0.328 |
LIG_CaM_NSCaTE_8 | 184 | 191 | PF13499 | 0.465 |
LIG_Clathr_ClatBox_1 | 298 | 302 | PF01394 | 0.440 |
LIG_Clathr_ClatBox_1 | 306 | 310 | PF01394 | 0.405 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.514 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.280 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.446 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.414 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.359 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.375 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.441 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.444 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.530 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.409 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.355 |
LIG_KLC1_Yacidic_2 | 120 | 124 | PF13176 | 0.442 |
LIG_LIR_Apic_2 | 410 | 414 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 211 | 217 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 286 | 296 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 326 | 336 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.351 |
LIG_Pex14_1 | 81 | 85 | PF04695 | 0.354 |
LIG_Rb_LxCxE_1 | 90 | 107 | PF01857 | 0.461 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.360 |
LIG_SH2_SRC | 412 | 415 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.372 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.372 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.338 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.421 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 25 | 32 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 297 | 302 | PF11976 | 0.349 |
LIG_TRAF2_1 | 117 | 120 | PF00917 | 0.347 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.401 |
LIG_TRFH_1 | 362 | 366 | PF08558 | 0.372 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.512 |
MOD_CDC14_SPxK_1 | 365 | 368 | PF00782 | 0.291 |
MOD_CDK_SPxK_1 | 362 | 368 | PF00069 | 0.338 |
MOD_CDK_SPxK_1 | 57 | 63 | PF00069 | 0.441 |
MOD_CDK_SPxxK_3 | 219 | 226 | PF00069 | 0.289 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.667 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.586 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.576 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.633 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.468 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.518 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.542 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.404 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.301 |
MOD_GlcNHglycan | 124 | 128 | PF01048 | 0.621 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.663 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.707 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.679 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.553 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.389 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.719 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.596 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.429 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.455 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.441 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.403 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.594 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.496 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.468 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.509 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.502 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.488 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.439 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.340 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.423 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.316 |
MOD_OFUCOSY | 41 | 48 | PF10250 | 0.366 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.362 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.404 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.404 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.597 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.467 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.445 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.441 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.564 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.310 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.421 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.460 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.395 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.705 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.597 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.290 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.338 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.441 |
MOD_SUMO_rev_2 | 100 | 110 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 244 | 249 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 86 | 91 | PF00179 | 0.321 |
TRG_DiLeu_BaEn_1 | 201 | 206 | PF01217 | 0.424 |
TRG_DiLeu_BaEn_1 | 430 | 435 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 229 | 234 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 64 | 69 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 313 | 317 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILD7 | Leptomonas seymouri | 59% | 98% |
A0A1X0NTS2 | Trypanosomatidae | 35% | 100% |
A0A3Q8IMS6 | Leishmania donovani | 24% | 100% |
A0A3S7WWY0 | Leishmania donovani | 89% | 100% |
A0A3S7WYG1 | Leishmania donovani | 24% | 100% |
A4HZP7 | Leishmania infantum | 89% | 100% |
A4I0X7 | Leishmania infantum | 25% | 100% |
A4I0X8 | Leishmania infantum | 25% | 98% |
E9AWY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AWY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4QAJ2 | Leishmania major | 26% | 97% |
Q4QAJ3 | Leishmania major | 25% | 100% |
Q4QBX6 | Leishmania major | 87% | 100% |