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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005777 | peroxisome | 6 | 1 |
GO:0005778 | peroxisomal membrane | 6 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0020015 | glycosome | 7 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031903 | microbody membrane | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0046860 | glycosome membrane | 7 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990351 | transporter complex | 2 | 1 |
GO:1990429 | peroxisomal importomer complex | 3 | 1 |
Related structures:
AlphaFold database: A4HA71
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 11 |
GO:0006625 | protein targeting to peroxisome | 5 | 11 |
GO:0006810 | transport | 3 | 11 |
GO:0006886 | intracellular protein transport | 4 | 11 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0007031 | peroxisome organization | 5 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0015919 | peroxisomal membrane transport | 5 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0016558 | protein import into peroxisome matrix | 5 | 11 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0033365 | protein localization to organelle | 5 | 11 |
GO:0043574 | peroxisomal transport | 4 | 11 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 11 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0046907 | intracellular transport | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0051649 | establishment of localization in cell | 3 | 11 |
GO:0055085 | transmembrane transport | 2 | 11 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0071806 | protein transmembrane transport | 3 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0072594 | establishment of protein localization to organelle | 4 | 11 |
GO:0072662 | protein localization to peroxisome | 6 | 11 |
GO:0072663 | establishment of protein localization to peroxisome | 5 | 11 |
GO:0006513 | protein monoubiquitination | 8 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0008022 | obsolete protein C-terminus binding | 3 | 11 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.271 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.242 |
DEG_APCC_DBOX_1 | 347 | 355 | PF00400 | 0.296 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.580 |
DOC_CDC14_PxL_1 | 96 | 104 | PF14671 | 0.534 |
DOC_CKS1_1 | 136 | 141 | PF01111 | 0.490 |
DOC_MAPK_gen_1 | 122 | 131 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 229 | 237 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 229 | 237 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 348 | 355 | PF00069 | 0.253 |
DOC_MAPK_NFAT4_5 | 348 | 356 | PF00069 | 0.296 |
DOC_PP1_RVXF_1 | 122 | 129 | PF00149 | 0.442 |
DOC_PP1_RVXF_1 | 140 | 147 | PF00149 | 0.422 |
DOC_PP1_RVXF_1 | 357 | 364 | PF00149 | 0.315 |
DOC_PP2B_LxvP_1 | 131 | 134 | PF13499 | 0.478 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.441 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.499 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.243 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.183 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 254 | 260 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 326 | 331 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 399 | 403 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 438 | 444 | PF00244 | 0.305 |
LIG_Actin_WH2_2 | 190 | 208 | PF00022 | 0.383 |
LIG_APCC_ABBA_1 | 240 | 245 | PF00400 | 0.534 |
LIG_eIF4E_1 | 125 | 131 | PF01652 | 0.534 |
LIG_eIF4E_1 | 302 | 308 | PF01652 | 0.271 |
LIG_EVH1_1 | 381 | 385 | PF00568 | 0.501 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.603 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.250 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.245 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.537 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.511 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.271 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.464 |
LIG_LIR_Apic_2 | 311 | 316 | PF02991 | 0.253 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 77 | 87 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.456 |
LIG_LYPXL_yS_3 | 430 | 433 | PF13949 | 0.274 |
LIG_NRBOX | 125 | 131 | PF00104 | 0.496 |
LIG_PDZ_Class_2 | 456 | 461 | PF00595 | 0.342 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.534 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.491 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.270 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.302 |
LIG_SH2_PTP2 | 286 | 289 | PF00017 | 0.408 |
LIG_SH2_SRC | 286 | 289 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.576 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.482 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.429 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.399 |
LIG_SUMO_SIM_anti_2 | 207 | 212 | PF11976 | 0.491 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.453 |
LIG_UBA3_1 | 235 | 241 | PF00899 | 0.471 |
MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.383 |
MOD_CDK_SPK_2 | 334 | 339 | PF00069 | 0.183 |
MOD_CDK_SPK_2 | 369 | 374 | PF00069 | 0.464 |
MOD_CDK_SPxxK_3 | 135 | 142 | PF00069 | 0.534 |
MOD_CDK_SPxxK_3 | 312 | 319 | PF00069 | 0.296 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.555 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.566 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.344 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.456 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.517 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.470 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.359 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.326 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.384 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.486 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.334 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.572 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.562 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.544 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.597 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.548 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.305 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.371 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.357 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.365 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.583 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.490 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.446 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.508 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.367 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.338 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.258 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.499 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.541 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.534 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.562 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.383 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.185 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.589 |
MOD_PKA_1 | 326 | 332 | PF00069 | 0.253 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.496 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.260 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.419 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.534 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.183 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.334 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.526 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.440 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.468 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.183 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.487 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.536 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.469 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.491 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.243 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.183 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.494 |
MOD_SUMO_for_1 | 211 | 214 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 183 | 192 | PF00179 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.253 |
TRG_DiLeu_BaLyEn_6 | 97 | 102 | PF01217 | 0.383 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.568 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.253 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.471 |
TRG_NES_CRM1_1 | 299 | 309 | PF08389 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 281 | 285 | PF00026 | 0.256 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.693 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1T8 | Leptomonas seymouri | 70% | 100% |
A0A1X0P610 | Trypanosomatidae | 45% | 100% |
A0A3S5H767 | Leishmania donovani | 88% | 100% |
A0A422NUP5 | Trypanosoma rangeli | 44% | 100% |
A4HYE3 | Leishmania infantum | 88% | 100% |
D0A0S8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AS76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QD90 | Leishmania major | 88% | 100% |
V5BED1 | Trypanosoma cruzi | 44% | 100% |