GPI anchor biosynthesis, GPI transamidase component Tta1 TTA1
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:0008303 | caspase complex | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042765 | GPI-anchor transamidase complex | 3 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905368 | peptidase complex | 3 | 1 |
GO:1905369 | endopeptidase complex | 4 | 1 |
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A4I877
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003923 | GPI-anchor transamidase activity | 6 | 1 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 1 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008234 | cysteine-type peptidase activity | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.672 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 295 | 297 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.589 |
DEG_APCC_DBOX_1 | 269 | 277 | PF00400 | 0.388 |
DEG_SCF_FBW7_1 | 70 | 77 | PF00400 | 0.549 |
DOC_CYCLIN_yCln2_LP_2 | 365 | 371 | PF00134 | 0.460 |
DOC_MAPK_gen_1 | 347 | 357 | PF00069 | 0.390 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.451 |
DOC_PP2B_LxvP_1 | 365 | 368 | PF13499 | 0.393 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.337 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.483 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.386 |
LIG_14-3-3_CanoR_1 | 135 | 144 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 245 | 255 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 261 | 266 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.724 |
LIG_Actin_WH2_2 | 300 | 317 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 333 | 349 | PF00022 | 0.439 |
LIG_BIR_III_4 | 211 | 215 | PF00653 | 0.317 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.449 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.396 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.414 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.437 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.449 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.515 |
LIG_GBD_Chelix_1 | 373 | 381 | PF00786 | 0.399 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 129 | 136 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 25 | 36 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 330 | 340 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 32 | 37 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.435 |
LIG_MYND_1 | 359 | 363 | PF01753 | 0.374 |
LIG_MYND_1 | 95 | 99 | PF01753 | 0.401 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.370 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.371 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.692 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.497 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.378 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.383 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.473 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.371 |
LIG_SUMO_SIM_anti_2 | 375 | 381 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 272 | 278 | PF11976 | 0.380 |
LIG_TYR_ITSM | 127 | 134 | PF00017 | 0.372 |
LIG_WRC_WIRS_1 | 130 | 135 | PF05994 | 0.372 |
LIG_WRC_WIRS_1 | 283 | 288 | PF05994 | 0.342 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.379 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.489 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.388 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.398 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.434 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.420 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.401 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.698 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.652 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.532 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.675 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.633 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.470 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.597 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.695 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.373 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.449 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.410 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.463 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.488 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.404 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.416 |
MOD_NEK2_2 | 282 | 287 | PF00069 | 0.386 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.418 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.423 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.434 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.487 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.461 |
MOD_PKB_1 | 259 | 267 | PF00069 | 0.471 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.353 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.404 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.354 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.302 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.390 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.291 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.243 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.465 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.452 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.551 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.384 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 258 | 261 | PF00400 | 0.454 |
TRG_ER_diLys_1 | 415 | 418 | PF00400 | 0.689 |
TRG_Pf-PMV_PEXEL_1 | 392 | 396 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 58 | 62 | PF00026 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I345 | Leptomonas seymouri | 56% | 97% |
A0A1X0NT15 | Trypanosomatidae | 27% | 100% |
A0A3S5IR84 | Trypanosoma rangeli | 31% | 100% |
A0A3S7X5V4 | Leishmania donovani | 100% | 100% |
A4HKP6 | Leishmania braziliensis | 77% | 100% |
D0AAE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9B335 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q519 | Leishmania major | 90% | 100% |
V5AUS2 | Trypanosoma cruzi | 29% | 96% |