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:0005739 | mitochondrion | 5 | 1 |
GO:0017087 | mitochondrial processing peptidase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 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:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A0A451EJB9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:0006810 | transport | 3 | 1 |
GO:0006839 | mitochondrial transport | 4 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0030150 | protein import into mitochondrial matrix | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 1 |
GO:0070585 | protein localization to mitochondrion | 6 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071806 | protein transmembrane transport | 3 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 1 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004175 | endopeptidase activity | 4 | 11 |
GO:0004222 | metalloendopeptidase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0008237 | metallopeptidase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.279 |
CLV_C14_Caspase3-7 | 429 | 433 | PF00656 | 0.371 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.335 |
CLV_PCSK_FUR_1 | 143 | 147 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.335 |
CLV_PCSK_PC7_1 | 141 | 147 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.252 |
DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.407 |
DEG_SCF_FBW7_2 | 331 | 338 | PF00400 | 0.321 |
DOC_CKS1_1 | 332 | 337 | PF01111 | 0.303 |
DOC_PP4_FxxP_1 | 332 | 335 | PF00568 | 0.301 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.245 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.337 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.339 |
DOC_USP7_UBL2_3 | 200 | 204 | PF12436 | 0.384 |
DOC_USP7_UBL2_3 | 390 | 394 | PF12436 | 0.327 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 91 | 101 | PF00244 | 0.287 |
LIG_Actin_WH2_2 | 424 | 442 | PF00022 | 0.454 |
LIG_BRCT_BRCA1_1 | 481 | 485 | PF00533 | 0.443 |
LIG_CtBP_PxDLS_1 | 436 | 440 | PF00389 | 0.455 |
LIG_CtBP_PxDLS_1 | 468 | 472 | PF00389 | 0.516 |
LIG_eIF4E_1 | 336 | 342 | PF01652 | 0.288 |
LIG_eIF4E_1 | 466 | 472 | PF01652 | 0.493 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.406 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.410 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.569 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.362 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.329 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.454 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.394 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.228 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.201 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.254 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.446 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.321 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.388 |
LIG_GBD_Chelix_1 | 198 | 206 | PF00786 | 0.304 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 444 | 454 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.302 |
LIG_PCNA_yPIPBox_3 | 358 | 369 | PF02747 | 0.367 |
LIG_PCNA_yPIPBox_3 | 68 | 81 | PF02747 | 0.245 |
LIG_Rb_pABgroove_1 | 368 | 376 | PF01858 | 0.440 |
LIG_SH2_CRK | 215 | 219 | PF00017 | 0.245 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.283 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.324 |
LIG_SH2_CRK | 466 | 470 | PF00017 | 0.579 |
LIG_SH2_PTP2 | 210 | 213 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.279 |
LIG_SH3_1 | 313 | 319 | PF00018 | 0.489 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.279 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.430 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.492 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.547 |
LIG_SUMO_SIM_anti_2 | 467 | 473 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 129 | 137 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 467 | 473 | PF11976 | 0.591 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.343 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.424 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.278 |
LIG_TYR_ITIM | 35 | 40 | PF00017 | 0.312 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.301 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.385 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.595 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.315 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.319 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.405 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.245 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.397 |
MOD_Cter_Amidation | 418 | 421 | PF01082 | 0.333 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.279 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.286 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.226 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.488 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.372 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.590 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.371 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.245 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.319 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.389 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.285 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.433 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.245 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.414 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.366 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.550 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.260 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.310 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.570 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.354 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.377 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.354 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.515 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.245 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.532 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.434 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.287 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.245 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.429 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.315 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.290 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.393 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.245 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.319 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.350 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.245 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.430 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.362 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.407 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.411 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.585 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.339 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.402 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.312 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.339 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.608 |
MOD_SUMO_for_1 | 389 | 392 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 387 | 396 | PF00179 | 0.357 |
TRG_DiLeu_BaEn_1 | 162 | 167 | PF01217 | 0.245 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.306 |
TRG_DiLeu_BaEn_4 | 337 | 343 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 248 | 253 | PF01217 | 0.384 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.579 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.330 |
TRG_NES_CRM1_1 | 414 | 426 | PF08389 | 0.332 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P575 | Leptomonas seymouri | 83% | 100% |
A0A0N1PEB5 | Leptomonas seymouri | 30% | 100% |
A0A0S4IUJ1 | Bodo saltans | 53% | 96% |
A0A0S4KFV6 | Bodo saltans | 31% | 98% |
A0A1X0NHX2 | Trypanosomatidae | 29% | 96% |
A0A1X0P2L6 | Trypanosomatidae | 70% | 96% |
A0A3S7X938 | Leishmania donovani | 30% | 100% |
A0A422N9N5 | Trypanosoma rangeli | 28% | 100% |
A0A422NGW3 | Trypanosoma rangeli | 69% | 100% |
A4HMG0 | Leishmania braziliensis | 30% | 100% |
A4HRI8 | Leishmania infantum | 100% | 100% |
A4IB31 | Leishmania infantum | 30% | 100% |
C9ZNM7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZXM0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 70% | 100% |
E9AC56 | Leishmania major | 97% | 100% |
E9AEW1 | Leishmania major | 30% | 100% |
E9AJF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9B617 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O04308 | Arabidopsis thaliana | 25% | 99% |
O05945 | Rickettsia prowazekii (strain Madrid E) | 21% | 100% |
O32965 | Mycobacterium leprae (strain TN) | 25% | 100% |
O75439 | Homo sapiens | 35% | 100% |
O86835 | Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) | 22% | 100% |
O94745 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 98% |
P07256 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 100% |
P0A5S9 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 24% | 100% |
P10507 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
P11913 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 33% | 100% |
P11914 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P20069 | Rattus norvegicus | 27% | 94% |
P22695 | Homo sapiens | 21% | 100% |
P23004 | Bos taurus | 22% | 100% |
P29677 | Solanum tuberosum | 25% | 98% |
P31800 | Bos taurus | 33% | 100% |
P31930 | Homo sapiens | 33% | 100% |
P32551 | Rattus norvegicus | 20% | 100% |
P43264 | Euglena gracilis | 40% | 100% |
P97997 | Blastocladiella emersonii | 25% | 100% |
P98080 | Caenorhabditis elegans | 28% | 100% |
P9WHT4 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 24% | 100% |
P9WHT5 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 24% | 100% |
Q00302 | Blastocladiella emersonii | 34% | 100% |
Q03346 | Rattus norvegicus | 36% | 100% |
Q04805 | Bacillus subtilis (strain 168) | 25% | 100% |
Q0P5M8 | Bos taurus | 28% | 94% |
Q10713 | Homo sapiens | 27% | 94% |
Q1RJ61 | Rickettsia bellii (strain RML369-C) | 22% | 100% |
Q23295 | Caenorhabditis elegans | 34% | 100% |
Q3SZ71 | Bos taurus | 37% | 100% |
Q42290 | Arabidopsis thaliana | 35% | 93% |
Q4UML9 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 22% | 100% |
Q4W6B5 | Dictyostelium discoideum | 32% | 100% |
Q54F93 | Dictyostelium discoideum | 23% | 100% |
Q5R513 | Pongo abelii | 28% | 94% |
Q5REK3 | Pongo abelii | 34% | 100% |
Q68FY0 | Rattus norvegicus | 32% | 100% |
Q92IX7 | Rickettsia conorii (strain ATCC VR-613 / Malish 7) | 22% | 100% |
Q9CXT8 | Mus musculus | 36% | 100% |
Q9CZ13 | Mus musculus | 32% | 100% |
Q9DC61 | Mus musculus | 27% | 94% |
Q9P7X1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
Q9Y8B5 | Lentinula edodes | 36% | 100% |
Q9ZU25 | Arabidopsis thaliana | 25% | 98% |
V5BGV2 | Trypanosoma cruzi | 29% | 100% |
V5BH27 | Trypanosoma cruzi | 70% | 100% |