Tricarboxylic acid cycle, fumarate hydratase
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. | yes | yes: 25 |
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:0005737 | cytoplasm | 2 | 1 |
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 | 1 |
Related structures:
AlphaFold database: A0A3S7WY69
Term | Name | Level | Count |
---|---|---|---|
GO:0006091 | generation of precursor metabolites and energy | 3 | 10 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006099 | tricarboxylic acid cycle | 3 | 1 |
GO:0006106 | fumarate metabolic process | 7 | 1 |
GO:0006108 | malate metabolic process | 7 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0043648 | dicarboxylic acid metabolic process | 6 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004333 | fumarate hydratase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0016829 | lyase activity | 2 | 11 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 11 |
GO:0016836 | hydro-lyase activity | 4 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0051536 | iron-sulfur cluster binding | 3 | 11 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 11 |
GO:0051540 | metal cluster binding | 2 | 11 |
GO:0005515 | protein binding | 2 | 1 |
GO:0042802 | identical protein binding | 3 | 1 |
GO:0042803 | protein homodimerization activity | 4 | 1 |
GO:0046983 | protein dimerization activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 87 | 91 | PF00656 | 0.412 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.459 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.409 |
CLV_Separin_Metazoa | 47 | 51 | PF03568 | 0.574 |
DEG_APCC_DBOX_1 | 331 | 339 | PF00400 | 0.452 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.612 |
DOC_CKS1_1 | 365 | 370 | PF01111 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 365 | 371 | PF00134 | 0.554 |
DOC_MAPK_gen_1 | 150 | 161 | PF00069 | 0.523 |
DOC_MAPK_gen_1 | 337 | 345 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 366 | 374 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 454 | 461 | PF00069 | 0.412 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.412 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.606 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.426 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.524 |
DOC_USP7_UBL2_3 | 479 | 483 | PF12436 | 0.479 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 154 | 161 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 315 | 321 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 391 | 397 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 72 | 79 | PF00244 | 0.557 |
LIG_Actin_WH2_2 | 64 | 82 | PF00022 | 0.419 |
LIG_AP2alpha_1 | 458 | 462 | PF02296 | 0.412 |
LIG_AP2alpha_2 | 456 | 458 | PF02296 | 0.431 |
LIG_APCC_ABBA_1 | 161 | 166 | PF00400 | 0.412 |
LIG_APCC_ABBA_1 | 455 | 460 | PF00400 | 0.412 |
LIG_APCC_Cbox_2 | 92 | 98 | PF00515 | 0.343 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 443 | 447 | PF00533 | 0.412 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.524 |
LIG_deltaCOP1_diTrp_1 | 522 | 532 | PF00928 | 0.412 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.406 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.479 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.524 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.409 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.412 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.412 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.412 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.479 |
LIG_Integrin_RGD_1 | 126 | 128 | PF01839 | 0.479 |
LIG_LIR_Gen_1 | 11 | 18 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 186 | 193 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 32 | 43 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 456 | 462 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 544 | 549 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 61 | 71 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 92 | 100 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 276 | 280 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 530 | 535 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 544 | 549 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.399 |
LIG_PDZ_Class_3 | 544 | 549 | PF00595 | 0.479 |
LIG_Pex14_2 | 458 | 462 | PF04695 | 0.412 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.547 |
LIG_SH2_CRK | 432 | 436 | PF00017 | 0.412 |
LIG_SH2_PTP2 | 35 | 38 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 155 | 159 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 187 | 191 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.412 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.479 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.412 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.510 |
LIG_SH3_4 | 268 | 275 | PF00018 | 0.524 |
LIG_SH3_4 | 419 | 426 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 34 | 40 | PF11976 | 0.496 |
LIG_UBA3_1 | 76 | 81 | PF00899 | 0.440 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.578 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.621 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.412 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.526 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.412 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.443 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.345 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.411 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.550 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.412 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.511 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.485 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.455 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.404 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.429 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.327 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.338 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.522 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.519 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.485 |
MOD_N-GLC_1 | 475 | 480 | PF02516 | 0.412 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.417 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.412 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.412 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.226 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.524 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.409 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.485 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.557 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.473 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.412 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.412 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.440 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.412 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.412 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.412 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.412 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.543 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.387 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.412 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.409 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.543 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.335 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.383 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.524 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.412 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.412 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.262 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.524 |
MOD_SUMO_rev_2 | 162 | 169 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 202 | 211 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 264 | 273 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 512 | 519 | PF00179 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 106 | 111 | PF01217 | 0.557 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 4 | 9 | PF01217 | 0.687 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.477 |
TRG_NES_CRM1_1 | 506 | 518 | PF08389 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 219 | 223 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 278 | 283 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 29 | 34 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I631 | Leptomonas seymouri | 59% | 97% |
A0A0N1PCN7 | Leptomonas seymouri | 85% | 100% |
A0A1X0NIU7 | Trypanosomatidae | 76% | 99% |
A0A1X0NZZ8 | Trypanosomatidae | 61% | 99% |
A0A3R7N408 | Trypanosoma rangeli | 74% | 99% |
A0A3S5IRI9 | Trypanosoma rangeli | 59% | 97% |
A2CIN0 | Leishmania infantum | 60% | 100% |
A2CIN8 | Leishmania donovani | 60% | 97% |
A4HD88 | Leishmania braziliensis | 92% | 100% |
A4HHJ6 | Leishmania braziliensis | 63% | 100% |
C9ZLE3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 97% |
D0A701 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 76% | 99% |
E9AE57 | Leishmania major | 60% | 100% |
E9AH43 | Leishmania infantum | 100% | 100% |
E9AWM1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
P0AC33 | Escherichia coli (strain K12) | 61% | 100% |
P0AC34 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 61% | 100% |
P14407 | Escherichia coli (strain K12) | 63% | 100% |
P40720 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 61% | 95% |
Q04718 | Geobacillus stearothermophilus | 23% | 100% |
Q4QAU9 | Leishmania major | 98% | 100% |
Q8X4P8 | Escherichia coli O157:H7 | 60% | 100% |
V5BGH8 | Trypanosoma cruzi | 60% | 97% |
V5DSN1 | Trypanosoma cruzi | 74% | 99% |