Align glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized)
to candidate Ga0059261_1680 Ga0059261_1680 NAD-dependent aldehyde dehydrogenases
Query= BRENDA::Q88RC0 (480 letters) >FitnessBrowser__Korea:Ga0059261_1680 Length = 469 Score = 285 bits (730), Expect = 2e-81 Identities = 163/451 (36%), Positives = 251/451 (55%), Gaps = 7/451 (1%) Query: 26 QTIKVTNPATGEVIGTVPKMGTAETRRAIEAADKALPAWRALTAKERSAKLRRWFELMIE 85 +T V +PATG P TA+ A+ AA +A P W A ++R+A + + + Sbjct: 17 ETFPVIDPATGRPFADAPLASTADLDAAVAAARRAFPGWAATPIEDRAAAILAIADSIEA 76 Query: 86 NQDDLARLMTTEQGKPLAEAKGEIAYAASFIEWFAEEAKRIYGDTIPGHQPDKRLIVIKQ 145 +D+LARL++ EQGKP+ A GEI A + W A + R+ V ++ Sbjct: 77 AKDELARLLSAEQGKPVPNAVGEIMGA---LAWARATAGLRPAVDVLKDDDSVRVEVHRK 133 Query: 146 PIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLKPASQTPYSALALVELAHRAGIPAGV 205 P+GV A+I+PWNFP + P L AG T+V+KP+S TP +AL +VE+A+ A +P GV Sbjct: 134 PLGVVASISPWNFPVMIAIWHIIPGLVAGNTVVMKPSSFTPLAALRMVEIAN-AHLPPGV 192 Query: 206 LSVVTGSAGEVGGELTGNSLVRKLSFTGSTEIGRQLMEECAKDIKKVSLELGGNAPFIVF 265 L+ VTG E+G + + + K+ FTGST GR +M + A ++K+++LELGGN IV Sbjct: 193 LNSVTGEV-EIGRAIASHPGIDKIVFTGSTPTGRSIMADGAANLKRLTLELGGNDAAIVL 251 Query: 266 DDADLDKAVEGAIISKYRNNGQTCVCANRIYVQDGVYDAFAEKLAAAVAKLKIGNGLEEG 325 DAD+DK + N+GQ C R+YV + ++DA AEKLA +G G + Sbjct: 252 PDADVDKVAAKIFAKAFGNSGQICAAVKRVYVHESIHDALAEKLAEMARTAVVGPGSDAA 311 Query: 326 TTTGPLIDGKAVAKVQEHIEDAVSKGAKVLSGGKLIEGN--FFEPTILVDVPKTAAVAKE 383 + GP+ + K V+ +DA + G + L+GG+ EG+ FF +++VDV + E Sbjct: 312 SQFGPVQNRKQFDLVRALADDARAHGGRFLAGGEAREGDGYFFPLSVVVDVTDGMRIVDE 371 Query: 384 ETFGPLAPLFRFKDEAEVIAMSNDTEFGLASYFYARDMSRVFRVAEALEYGMVGINTGLI 443 E FGP+ P+ R+ D + +A +N E GL ++ D + A+ LE G V +N Sbjct: 372 EQFGPILPVIRYSDPEDALARANANENGLGGSVWSADPAAALAFAQRLEAGTVWVNDHAS 431 Query: 444 SNEVAPFGGIKASGLGREGSKYGIEDYLEIK 474 + PFGG K SG+G E YG+E+Y++++ Sbjct: 432 ISPDVPFGGAKQSGVGTEFGLYGLEEYMQLQ 462 Lambda K H 0.317 0.134 0.384 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 566 Number of extensions: 31 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 480 Length of database: 469 Length adjustment: 33 Effective length of query: 447 Effective length of database: 436 Effective search space: 194892 Effective search space used: 194892 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory