GPI anchor biosynthesis, GPI transamidase component Tta2 TTA2
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0008303 | caspase complex | 5 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042765 | GPI-anchor transamidase complex | 3 | 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:0098796 | membrane protein complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
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 |
Related structures:
AlphaFold database: A4ICR9
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 | 157 | 161 | PF00656 | 0.585 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.363 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.708 |
DEG_APCC_DBOX_1 | 350 | 358 | PF00400 | 0.536 |
DEG_APCC_DBOX_1 | 36 | 44 | PF00400 | 0.266 |
DEG_MDM2_SWIB_1 | 457 | 465 | PF02201 | 0.447 |
DEG_ODPH_VHL_1 | 244 | 256 | PF01847 | 0.441 |
DEG_ODPH_VHL_1 | 317 | 329 | PF01847 | 0.599 |
DEG_SPOP_SBC_1 | 337 | 341 | PF00917 | 0.662 |
DOC_CDC14_PxL_1 | 315 | 323 | PF14671 | 0.590 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.467 |
DOC_CYCLIN_RxL_1 | 296 | 305 | PF00134 | 0.674 |
DOC_CYCLIN_yCln2_LP_2 | 23 | 29 | PF00134 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 321 | 327 | PF00134 | 0.573 |
DOC_CYCLIN_yCln2_LP_2 | 369 | 375 | PF00134 | 0.642 |
DOC_CYCLIN_yCln2_LP_2 | 411 | 417 | PF00134 | 0.373 |
DOC_MAPK_DCC_7 | 408 | 417 | PF00069 | 0.562 |
DOC_MAPK_DCC_7 | 91 | 100 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 408 | 417 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 21 | 30 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 408 | 417 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 91 | 100 | PF00069 | 0.519 |
DOC_MAPK_RevD_3 | 200 | 215 | PF00069 | 0.442 |
DOC_PP1_RVXF_1 | 251 | 257 | PF00149 | 0.330 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.660 |
DOC_PP2B_LxvP_1 | 301 | 304 | PF13499 | 0.549 |
DOC_PP2B_LxvP_1 | 321 | 324 | PF13499 | 0.400 |
DOC_PP2B_LxvP_1 | 369 | 372 | PF13499 | 0.588 |
DOC_PP2B_LxvP_1 | 411 | 414 | PF13499 | 0.373 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.502 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.464 |
LIG_14-3-3_CanoR_1 | 169 | 178 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 282 | 287 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 335 | 344 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 366 | 372 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 399 | 404 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 44 | 48 | PF00244 | 0.442 |
LIG_AP_GAE_1 | 120 | 126 | PF02883 | 0.429 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.648 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.648 |
LIG_BRCT_BRCA1_1 | 279 | 283 | PF00533 | 0.674 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.568 |
LIG_EH_1 | 24 | 28 | PF12763 | 0.305 |
LIG_EH1_1 | 255 | 263 | PF00400 | 0.266 |
LIG_eIF4E_1 | 406 | 412 | PF01652 | 0.562 |
LIG_EVH1_2 | 96 | 100 | PF00568 | 0.482 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.374 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.473 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.355 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.496 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.652 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.436 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.353 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.695 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.539 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.669 |
LIG_HP1_1 | 240 | 244 | PF01393 | 0.441 |
LIG_LIR_Apic_2 | 285 | 290 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 120 | 131 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 280 | 290 | PF02991 | 0.699 |
LIG_LIR_Gen_1 | 370 | 381 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 404 | 414 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 402 | 406 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 455 | 460 | PF02991 | 0.363 |
LIG_Pex14_1 | 137 | 141 | PF04695 | 0.440 |
LIG_Pex14_2 | 30 | 34 | PF04695 | 0.447 |
LIG_Pex14_2 | 428 | 432 | PF04695 | 0.512 |
LIG_Pex14_2 | 457 | 461 | PF04695 | 0.335 |
LIG_RPA_C_Fungi | 164 | 176 | PF08784 | 0.457 |
LIG_SH2_CRK | 269 | 273 | PF00017 | 0.480 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.486 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.489 |
LIG_SH2_CRK | 406 | 410 | PF00017 | 0.547 |
LIG_SH2_NCK_1 | 287 | 291 | PF00017 | 0.525 |
LIG_SH2_SRC | 273 | 276 | PF00017 | 0.532 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.589 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 462 | 466 | PF00017 | 0.519 |
LIG_SH2_STAT3 | 129 | 132 | PF00017 | 0.591 |
LIG_SH2_STAT3 | 297 | 300 | PF00017 | 0.609 |
LIG_SH2_STAT3 | 333 | 336 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.685 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.690 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.581 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.335 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.475 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.634 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.625 |
LIG_SUMO_SIM_anti_2 | 201 | 206 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 359 | 365 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 185 | 196 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 201 | 206 | PF11976 | 0.237 |
LIG_SUMO_SIM_par_1 | 390 | 397 | PF11976 | 0.545 |
LIG_TRFH_1 | 182 | 186 | PF08558 | 0.355 |
LIG_TYR_ITIM | 371 | 376 | PF00017 | 0.496 |
LIG_TYR_ITIM | 460 | 465 | PF00017 | 0.473 |
LIG_WRC_WIRS_1 | 197 | 202 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 303 | 308 | PF05994 | 0.573 |
LIG_WRC_WIRS_1 | 31 | 36 | PF05994 | 0.408 |
MOD_CDK_SPxxK_3 | 401 | 408 | PF00069 | 0.603 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.511 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.480 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.397 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.649 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.544 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.672 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.518 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.429 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.423 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.237 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.511 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.671 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.641 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.666 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.390 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.530 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.454 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.495 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.587 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.679 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.499 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.507 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.436 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.448 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.408 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.233 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.355 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.447 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.651 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.395 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.366 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.529 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.747 |
MOD_NEK2_2 | 39 | 44 | PF00069 | 0.482 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.498 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.643 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.518 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.511 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.580 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.614 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.562 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.480 |
MOD_Plk_2-3 | 108 | 114 | PF00069 | 0.533 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.499 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.453 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.459 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.408 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.598 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.651 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.596 |
TRG_DiLeu_BaLyEn_6 | 407 | 412 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 407 | 410 | PF00400 | 0.593 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Y0 | Leptomonas seymouri | 63% | 96% |
A0A1X0P8I4 | Trypanosomatidae | 38% | 100% |
A0A3Q8IIQ8 | Leishmania donovani | 100% | 100% |
A0A422P255 | Trypanosoma rangeli | 37% | 100% |
A4HNS5 | Leishmania braziliensis | 80% | 100% |
D0A2N5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9ASI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q211 | Leishmania major | 93% | 100% |
V5BZX2 | Trypanosoma cruzi | 38% | 100% |