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: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: Q4QBX6
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 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043169 | cation binding | 3 | 17 |
GO:0046872 | metal ion binding | 4 | 17 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
GO:0005509 | calcium ion binding | 5 | 11 |
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_NRD_NRD_1 | 275 | 277 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.461 |
CLV_PCSK_FUR_1 | 331 | 335 | PF00082 | 0.285 |
CLV_PCSK_FUR_1 | 405 | 409 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.439 |
DOC_ANK_TNKS_1 | 38 | 45 | PF00023 | 0.342 |
DOC_CKS1_1 | 58 | 63 | PF01111 | 0.425 |
DOC_CYCLIN_RxL_1 | 330 | 340 | PF00134 | 0.304 |
DOC_CYCLIN_yCln2_LP_2 | 144 | 150 | PF00134 | 0.547 |
DOC_MAPK_gen_1 | 404 | 412 | PF00069 | 0.330 |
DOC_PP1_RVXF_1 | 230 | 237 | PF00149 | 0.472 |
DOC_PP1_RVXF_1 | 406 | 413 | PF00149 | 0.328 |
DOC_PP4_FxxP_1 | 212 | 215 | PF00568 | 0.352 |
DOC_PP4_FxxP_1 | 362 | 365 | PF00568 | 0.427 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.359 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.444 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 185 | 195 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.388 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.499 |
LIG_BRCT_BRCA1_1 | 260 | 264 | PF00533 | 0.315 |
LIG_CaM_NSCaTE_8 | 184 | 191 | PF13499 | 0.458 |
LIG_Clathr_ClatBox_1 | 298 | 302 | PF01394 | 0.414 |
LIG_Clathr_ClatBox_1 | 306 | 310 | PF01394 | 0.386 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.422 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.432 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.358 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.329 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.429 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.620 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.409 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.379 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.354 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.366 |
LIG_KLC1_Yacidic_2 | 120 | 124 | PF13176 | 0.423 |
LIG_LIR_Apic_2 | 211 | 215 | PF02991 | 0.351 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 411 | 415 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 326 | 336 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.422 |
LIG_Pex14_1 | 81 | 85 | PF04695 | 0.350 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.347 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.354 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.333 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.402 |
LIG_SUMO_SIM_par_1 | 25 | 32 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 297 | 302 | PF11976 | 0.332 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.387 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.514 |
MOD_CDK_SPxK_1 | 57 | 63 | PF00069 | 0.425 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.677 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.492 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.431 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.628 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.474 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.362 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.613 |
MOD_GlcNHglycan | 124 | 128 | PF01048 | 0.672 |
MOD_GlcNHglycan | 131 | 135 | PF01048 | 0.751 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.654 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.393 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.369 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.420 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.451 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.437 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.436 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.483 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.482 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.473 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.536 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.534 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.447 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.381 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.454 |
MOD_OFUCOSY | 41 | 48 | PF10250 | 0.345 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.345 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.481 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.388 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.501 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.452 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.297 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.461 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.553 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.415 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.386 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.664 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.796 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.425 |
MOD_SUMO_for_1 | 128 | 131 | PF00179 | 0.517 |
MOD_SUMO_for_1 | 385 | 388 | PF00179 | 0.342 |
MOD_SUMO_rev_2 | 100 | 110 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 244 | 249 | PF00179 | 0.340 |
TRG_DiLeu_BaEn_1 | 201 | 206 | PF01217 | 0.461 |
TRG_DiLeu_BaEn_1 | 431 | 436 | PF01217 | 0.373 |
TRG_DiLeu_BaLyEn_6 | 229 | 234 | PF01217 | 0.311 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 64 | 69 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 313 | 317 | PF00026 | 0.310 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILD7 | Leptomonas seymouri | 59% | 99% |
A0A1X0NTS2 | Trypanosomatidae | 34% | 100% |
A0A3Q8IMS6 | Leishmania donovani | 24% | 100% |
A0A3S5H5B1 | Leishmania donovani | 22% | 76% |
A0A3S7WWY0 | Leishmania donovani | 90% | 100% |
A0A3S7WYG1 | Leishmania donovani | 27% | 100% |
A4HS49 | Leishmania infantum | 22% | 76% |
A4HZP7 | Leishmania infantum | 90% | 100% |
A4I0X7 | Leishmania infantum | 25% | 100% |
A4I0X8 | Leishmania infantum | 27% | 100% |
E9AVK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9AWY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AWY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
O97201 | Leishmania major | 23% | 76% |
Q4QAJ2 | Leishmania major | 27% | 100% |
Q4QAJ3 | Leishmania major | 25% | 100% |