Mitochondrial protein, Uncharacterized
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AH59
Term | Name | Level | Count |
---|---|---|---|
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0030656 | regulation of vitamin metabolic process | 5 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0062012 | regulation of small molecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0106064 | regulation of cobalamin metabolic process | 6 | 1 |
GO:1901401 | regulation of tetrapyrrole metabolic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016829 | lyase activity | 2 | 3 |
GO:0016830 | carbon-carbon lyase activity | 3 | 1 |
GO:0016833 | oxo-acid-lyase activity | 4 | 1 |
GO:0047777 | (S)-citramalyl-CoA lyase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.338 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.643 |
CLV_PCSK_FUR_1 | 144 | 148 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.395 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.760 |
DOC_CDC14_PxL_1 | 173 | 181 | PF14671 | 0.545 |
DOC_CKS1_1 | 25 | 30 | PF01111 | 0.634 |
DOC_CKS1_1 | 338 | 343 | PF01111 | 0.597 |
DOC_CYCLIN_yCln2_LP_2 | 418 | 424 | PF00134 | 0.305 |
DOC_MAPK_DCC_7 | 416 | 424 | PF00069 | 0.255 |
DOC_MAPK_gen_1 | 469 | 477 | PF00069 | 0.366 |
DOC_PP1_RVXF_1 | 158 | 165 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 334 | 337 | PF13499 | 0.511 |
DOC_PP4_FxxP_1 | 302 | 305 | PF00568 | 0.340 |
DOC_PP4_FxxP_1 | 392 | 395 | PF00568 | 0.509 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.664 |
DOC_USP7_UBL2_3 | 485 | 489 | PF12436 | 0.585 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 402 | 406 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 47 | 57 | PF00244 | 0.714 |
LIG_14-3-3_CterR_2 | 534 | 537 | PF00244 | 0.749 |
LIG_APCC_ABBA_1 | 89 | 94 | PF00400 | 0.496 |
LIG_BIR_III_2 | 239 | 243 | PF00653 | 0.499 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.543 |
LIG_BRCT_BRCA1_1 | 57 | 61 | PF00533 | 0.721 |
LIG_CaM_IQ_9 | 208 | 224 | PF13499 | 0.543 |
LIG_Clathr_ClatBox_1 | 410 | 414 | PF01394 | 0.372 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.748 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.474 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.385 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.475 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.678 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.387 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.394 |
LIG_LIR_Apic_2 | 290 | 294 | PF02991 | 0.398 |
LIG_LIR_Apic_2 | 389 | 395 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.516 |
LIG_LYPXL_yS_3 | 241 | 244 | PF13949 | 0.502 |
LIG_MYND_1 | 155 | 159 | PF01753 | 0.538 |
LIG_NRBOX | 263 | 269 | PF00104 | 0.417 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 431 | 435 | PF00017 | 0.421 |
LIG_SH2_PTP2 | 291 | 294 | PF00017 | 0.449 |
LIG_SH2_SRC | 253 | 256 | PF00017 | 0.498 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.414 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.524 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.510 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.626 |
LIG_SUMO_SIM_anti_2 | 303 | 310 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 184 | 191 | PF11976 | 0.485 |
LIG_TRAF2_1 | 101 | 104 | PF00917 | 0.602 |
LIG_TRAF2_1 | 404 | 407 | PF00917 | 0.421 |
LIG_TRAF2_1 | 433 | 436 | PF00917 | 0.255 |
LIG_UBA3_1 | 410 | 416 | PF00899 | 0.372 |
MOD_CDK_SPK_2 | 42 | 47 | PF00069 | 0.606 |
MOD_CDK_SPK_2 | 61 | 66 | PF00069 | 0.667 |
MOD_CDK_SPxK_1 | 42 | 48 | PF00069 | 0.609 |
MOD_CDK_SPxK_1 | 526 | 532 | PF00069 | 0.751 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.463 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.412 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.720 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.712 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.489 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.421 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.329 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.388 |
MOD_Cter_Amidation | 144 | 147 | PF01082 | 0.755 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.749 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.580 |
MOD_GlcNHglycan | 329 | 333 | PF01048 | 0.546 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.485 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.544 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.755 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.638 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.545 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.544 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.733 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.462 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.523 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.660 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.338 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.735 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.663 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.639 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.608 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.601 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.313 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.762 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.464 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.428 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.559 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.662 |
MOD_NEK2_2 | 278 | 283 | PF00069 | 0.386 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.540 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.588 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.599 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.732 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.421 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.653 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.692 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.621 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.418 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.393 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.620 |
MOD_Plk_2-3 | 349 | 355 | PF00069 | 0.519 |
MOD_Plk_2-3 | 454 | 460 | PF00069 | 0.372 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.655 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.378 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.418 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.714 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.709 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.362 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.328 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.545 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.760 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.374 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.751 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.666 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 146 | 151 | PF01217 | 0.702 |
TRG_DiLeu_BaLyEn_6 | 240 | 245 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 309 | 314 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 406 | 411 | PF01217 | 0.372 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.505 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.702 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.656 |
TRG_NLS_MonoExtC_3 | 196 | 201 | PF00514 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 403 | 407 | PF00026 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 409 | 414 | PF00026 | 0.342 |
TRG_Pf-PMV_PEXEL_1 | 83 | 88 | PF00026 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHZ0 | Leptomonas seymouri | 57% | 100% |
A0A1X0NVS5 | Trypanosomatidae | 31% | 100% |
A0A3S7WYJ5 | Leishmania donovani | 100% | 100% |
A4HDJ6 | Leishmania braziliensis | 74% | 99% |
C9ZWG8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AWY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
Q4QAI7 | Leishmania major | 89% | 100% |
V5DBJ5 | Trypanosoma cruzi | 35% | 100% |