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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 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:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9B4P6
Term | Name | Level | Count |
---|---|---|---|
GO:0006091 | generation of precursor metabolites and energy | 3 | 1 |
GO:0006120 | mitochondrial electron transport, NADH to ubiquinone | 7 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009060 | aerobic respiration | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010257 | NADH dehydrogenase complex assembly | 6 | 1 |
GO:0015980 | energy derivation by oxidation of organic compounds | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019646 | aerobic electron transport chain | 6 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022900 | electron transport chain | 4 | 1 |
GO:0022904 | respiratory electron transport chain | 5 | 1 |
GO:0032981 | mitochondrial respiratory chain complex I assembly | 7 | 1 |
GO:0033108 | mitochondrial respiratory chain complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0045333 | cellular respiration | 5 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0051082 | unfolded protein binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.707 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.518 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.534 |
DEG_APCC_DBOX_1 | 202 | 210 | PF00400 | 0.570 |
DEG_APCC_DBOX_1 | 377 | 385 | PF00400 | 0.489 |
DOC_CKS1_1 | 7 | 12 | PF01111 | 0.659 |
DOC_CYCLIN_RxL_1 | 122 | 136 | PF00134 | 0.539 |
DOC_CYCLIN_yCln2_LP_2 | 373 | 379 | PF00134 | 0.542 |
DOC_MAPK_gen_1 | 112 | 119 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 126 | 134 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 400 | 410 | PF00069 | 0.613 |
DOC_MAPK_MEF2A_6 | 112 | 119 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 126 | 134 | PF00069 | 0.441 |
DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.656 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.538 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.564 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.747 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 143 | 148 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 183 | 189 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 224 | 229 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 306 | 312 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 336 | 340 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 358 | 366 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 378 | 382 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 383 | 390 | PF00244 | 0.433 |
LIG_Actin_WH2_2 | 229 | 247 | PF00022 | 0.371 |
LIG_Actin_WH2_2 | 435 | 451 | PF00022 | 0.692 |
LIG_Actin_WH2_2 | 99 | 114 | PF00022 | 0.494 |
LIG_APCC_ABBA_1 | 30 | 35 | PF00400 | 0.709 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.725 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.495 |
LIG_CSL_BTD_1 | 256 | 259 | PF09270 | 0.597 |
LIG_deltaCOP1_diTrp_1 | 352 | 357 | PF00928 | 0.592 |
LIG_eIF4E_1 | 303 | 309 | PF01652 | 0.592 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.571 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.696 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.457 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.660 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.668 |
LIG_GBD_Chelix_1 | 228 | 236 | PF00786 | 0.529 |
LIG_LIR_Apic_2 | 253 | 259 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 283 | 294 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 462 | 470 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.641 |
LIG_LYPXL_yS_3 | 57 | 60 | PF13949 | 0.643 |
LIG_Pex14_1 | 357 | 361 | PF04695 | 0.500 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.719 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 11 | 15 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.711 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.584 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.720 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.641 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.603 |
LIG_SUMO_SIM_anti_2 | 116 | 121 | PF11976 | 0.423 |
LIG_SUMO_SIM_anti_2 | 90 | 97 | PF11976 | 0.499 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.598 |
LIG_WRC_WIRS_1 | 389 | 394 | PF05994 | 0.603 |
MOD_CDC14_SPxK_1 | 375 | 378 | PF00782 | 0.577 |
MOD_CDK_SPxK_1 | 372 | 378 | PF00069 | 0.569 |
MOD_CDK_SPxxK_3 | 329 | 336 | PF00069 | 0.579 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.718 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.691 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.529 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.619 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.520 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.587 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.645 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.666 |
MOD_CMANNOS | 353 | 356 | PF00535 | 0.605 |
MOD_Cter_Amidation | 265 | 268 | PF01082 | 0.645 |
MOD_DYRK1A_RPxSP_1 | 6 | 10 | PF00069 | 0.673 |
MOD_GlcNHglycan | 12 | 16 | PF01048 | 0.573 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.749 |
MOD_GlcNHglycan | 237 | 242 | PF01048 | 0.645 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.623 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.548 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.596 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.731 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.382 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.582 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.645 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.482 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.594 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.406 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.642 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.642 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.519 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.700 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.579 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.598 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.521 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.667 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.506 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.601 |
MOD_PK_1 | 113 | 119 | PF00069 | 0.488 |
MOD_PK_1 | 224 | 230 | PF00069 | 0.500 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.574 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.291 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.589 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.646 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.458 |
MOD_PKB_1 | 358 | 366 | PF00069 | 0.499 |
MOD_PKB_1 | 447 | 455 | PF00069 | 0.448 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.527 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.558 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.430 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.428 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.444 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.651 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.558 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.679 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.460 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.632 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.519 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.529 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.530 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.569 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.742 |
MOD_SUMO_rev_2 | 136 | 144 | PF00179 | 0.349 |
TRG_DiLeu_BaEn_1 | 91 | 96 | PF01217 | 0.549 |
TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 418 | 423 | PF01217 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.665 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.678 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.643 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.617 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZN2 | Leptomonas seymouri | 66% | 98% |
A0A0S4IVY0 | Bodo saltans | 24% | 100% |
A0A1X0P965 | Trypanosomatidae | 33% | 100% |
A0A3Q8IIA0 | Leishmania donovani | 92% | 100% |
A4HAI5 | Leishmania braziliensis | 80% | 100% |
E9AHS6 | Leishmania infantum | 92% | 100% |
Q4Q3D0 | Leishmania major | 89% | 100% |
V5BEX5 | Trypanosoma cruzi | 34% | 100% |