Glycosome membrane, Peroxin 16
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005778 | peroxisomal membrane | 6 | 10 |
GO:0016020 | membrane | 2 | 10 |
GO:0031090 | organelle membrane | 3 | 10 |
GO:0031903 | microbody membrane | 5 | 10 |
GO:0042579 | microbody | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0098588 | bounding membrane of organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005777 | peroxisome | 6 | 1 |
GO:0020015 | glycosome | 7 | 1 |
Related structures:
AlphaFold database: A4HWH7
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 10 |
GO:0007031 | peroxisome organization | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.786 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.472 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.333 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.607 |
DEG_APCC_DBOX_1 | 29 | 37 | PF00400 | 0.610 |
DEG_APCC_DBOX_1 | 502 | 510 | PF00400 | 0.502 |
DEG_SPOP_SBC_1 | 467 | 471 | PF00917 | 0.646 |
DOC_ANK_TNKS_1 | 47 | 54 | PF00023 | 0.467 |
DOC_CDC14_PxL_1 | 157 | 165 | PF14671 | 0.635 |
DOC_CYCLIN_yCln2_LP_2 | 315 | 321 | PF00134 | 0.358 |
DOC_MAPK_DCC_7 | 422 | 431 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 100 | 110 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 133 | 141 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 419 | 428 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 104 | 112 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 317 | 324 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 422 | 431 | PF00069 | 0.595 |
DOC_MAPK_RevD_3 | 158 | 173 | PF00069 | 0.631 |
DOC_PP2B_LxvP_1 | 248 | 251 | PF13499 | 0.583 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.407 |
DOC_PP2B_LxvP_1 | 343 | 346 | PF13499 | 0.417 |
DOC_PP4_FxxP_1 | 158 | 161 | PF00568 | 0.570 |
DOC_PP4_MxPP_1 | 486 | 489 | PF00568 | 0.617 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.559 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.530 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.803 |
LIG_14-3-3_CanoR_1 | 100 | 108 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 133 | 137 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 176 | 182 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 62 | 67 | PF00244 | 0.473 |
LIG_Actin_RPEL_3 | 18 | 37 | PF02755 | 0.648 |
LIG_Actin_WH2_2 | 301 | 319 | PF00022 | 0.227 |
LIG_AP2alpha_2 | 512 | 514 | PF02296 | 0.506 |
LIG_Clathr_ClatBox_1 | 139 | 143 | PF01394 | 0.530 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.477 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.592 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.432 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.556 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.411 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.496 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.689 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.447 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.378 |
LIG_LIR_Apic_2 | 219 | 223 | PF02991 | 0.598 |
LIG_LIR_Apic_2 | 65 | 71 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 301 | 310 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 311 | 321 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 512 | 523 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 547 | 557 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 88 | 95 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 301 | 305 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 512 | 518 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.519 |
LIG_NRBOX | 412 | 418 | PF00104 | 0.360 |
LIG_Pex14_2 | 158 | 162 | PF04695 | 0.563 |
LIG_Pex14_2 | 527 | 531 | PF04695 | 0.598 |
LIG_PTB_Apo_2 | 501 | 508 | PF02174 | 0.544 |
LIG_PTB_Phospho_1 | 501 | 507 | PF10480 | 0.587 |
LIG_SH2_CRK | 220 | 224 | PF00017 | 0.697 |
LIG_SH2_CRK | 555 | 559 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 545 | 549 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 555 | 559 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.321 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.671 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.384 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.517 |
LIG_SUMO_SIM_anti_2 | 105 | 112 | PF11976 | 0.470 |
LIG_SUMO_SIM_anti_2 | 301 | 307 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 442 | 448 | PF11976 | 0.634 |
LIG_SUMO_SIM_par_1 | 138 | 143 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 442 | 448 | PF11976 | 0.632 |
LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.400 |
LIG_TRAF2_1 | 362 | 365 | PF00917 | 0.347 |
LIG_UBA3_1 | 139 | 146 | PF00899 | 0.447 |
LIG_UBA3_1 | 36 | 45 | PF00899 | 0.561 |
LIG_WRC_WIRS_1 | 554 | 559 | PF05994 | 0.382 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.515 |
MOD_CDK_SPK_2 | 179 | 184 | PF00069 | 0.662 |
MOD_CDK_SPxK_1 | 179 | 185 | PF00069 | 0.668 |
MOD_CDK_SPxK_1 | 368 | 374 | PF00069 | 0.482 |
MOD_CDK_SPxxK_3 | 179 | 186 | PF00069 | 0.671 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.758 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.639 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.530 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.523 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.681 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.382 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.502 |
MOD_CMANNOS | 401 | 404 | PF00535 | 0.465 |
MOD_Cter_Amidation | 255 | 258 | PF01082 | 0.378 |
MOD_Cter_Amidation | 98 | 101 | PF01082 | 0.265 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.585 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.556 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.414 |
MOD_GlcNHglycan | 228 | 232 | PF01048 | 0.427 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.436 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.350 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.560 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.628 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.713 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.376 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.699 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.463 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.343 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.496 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.585 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.741 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.636 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.377 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.665 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.308 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.358 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.284 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.550 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.693 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.769 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.530 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.530 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.544 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.513 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.358 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.313 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.530 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.742 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.668 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.542 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.803 |
MOD_SUMO_rev_2 | 364 | 369 | PF00179 | 0.523 |
TRG_DiLeu_BaEn_1 | 106 | 111 | PF01217 | 0.571 |
TRG_DiLeu_BaEn_1 | 117 | 122 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_1 | 335 | 340 | PF01217 | 0.303 |
TRG_DiLeu_BaLyEn_6 | 533 | 538 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.260 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.679 |
TRG_Pf-PMV_PEXEL_1 | 113 | 117 | PF00026 | 0.290 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4R8 | Leptomonas seymouri | 58% | 100% |
A0A1X0NUI4 | Trypanosomatidae | 36% | 100% |
A0A3Q8ICA1 | Leishmania donovani | 100% | 100% |
A4H843 | Leishmania braziliensis | 82% | 99% |
C9ZXX1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AQ78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
Q4QFA4 | Leishmania major | 95% | 100% |
V5DL46 | Trypanosoma cruzi | 34% | 100% |