Align glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized)
to candidate WP_043527583.1 JH15_RS05030 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::Q88RC0 (480 letters) >NCBI__GCF_000759345.1:WP_043527583.1 Length = 493 Score = 483 bits (1244), Expect = e-141 Identities = 235/480 (48%), Positives = 326/480 (67%), Gaps = 2/480 (0%) Query: 1 MQLKDAQLFRQQAYINGEWLDADNGQTIKVTNPATGEVIGTVPKMGTAETRRAIEAADKA 60 ++L D +LFRQ AY+ G+W D G+ VTNPA GEV+G +P + + R A++AA+ A Sbjct: 5 IKLSDPRLFRQHAYVGGKWTYGDGGREEAVTNPANGEVLGHIPWLEPDQIRAAVDAAEGA 64 Query: 61 LPAWRALTAKERSAKLRRWFELMIENQDDLARLMTTEQGKPLAEAKGEIAYAASFIEWFA 120 WRAL ER +L W +L++EN++DLA LMT EQGKPL +A+GE+ Y ASFI WFA Sbjct: 65 FANWRALRVDERCERLLAWHDLLLENREDLAILMTHEQGKPLPDARGEVEYGASFIRWFA 124 Query: 121 EEAKRIYGDTIPGHQPDKRLIVIKQPIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLK 180 EE KR +G TIP H P+ L IK+P+G+ A ITPWNFP AMITRKA A+AAGC +++K Sbjct: 125 EEGKRTFGQTIPSHIPNAALGTIKEPVGIAALITPWNFPLAMITRKAAAAMAAGCPVIVK 184 Query: 181 PASQTPYSALALVELAHRAGIPAGVLSVVTGSAGEVGGELTGNSLVRKLSFTGSTEIGRQ 240 PA +TP++ALAL ELA RA IPAG+ +VV G A +V L ++ LSFTGST +GR Sbjct: 185 PAGETPFTALALAELAERASIPAGIFNVVLGDAPQVSEVLCAEERIKALSFTGSTRVGRL 244 Query: 241 LMEECAKDIKKVSLELGGNAPFIVFDDADLDKAVEGAIISKYRNNGQTCVCANRIYVQDG 300 L+E+ A +K+VSLELGGNAPFIV D D +A A+ +K++ GQ C+ A+RI V + Sbjct: 245 LLEQSANSVKRVSLELGGNAPFIVGPDVDPKEAAFAAVSAKFQTGGQDCLAADRILVHES 304 Query: 301 VYDAFAEKLAAAVAKLKIGNGLEEGTTTGPLIDGKAVAKVQEHIEDAVSKGAKVLSG--G 358 V+DAF E A +A L +GNGL+ GPLI GKAV K ++DA+S+GA +++G Sbjct: 305 VHDAFVEHFAERMAALTVGNGLDSEIDLGPLIHGKAVEKAMGIVDDAISQGATLVAGDQS 364 Query: 359 KLIEGNFFEPTILVDVPKTAAVAKEETFGPLAPLFRFKDEAEVIAMSNDTEFGLASYFYA 418 + N+F P +L V + +V +EE F P+A + + + + + M+NDTE+GLA+Y Y Sbjct: 365 QAPGPNYFMPVLLTGVTPSMSVWREENFSPVAGITAYSTDDQALEMANDTEYGLAAYVYT 424 Query: 419 RDMSRVFRVAEALEYGMVGINTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEIKYLCI 478 D+ R++++ LEYGMV +N+ ++ PFGG+K SGLGREG GIE++LE KY C+ Sbjct: 425 HDIRRIWKMLRGLEYGMVAVNSVKMTGAPIPFGGVKQSGLGREGGTAGIEEFLETKYYCL 484 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: 639 Number of extensions: 22 Number of successful extensions: 2 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: 493 Length adjustment: 34 Effective length of query: 446 Effective length of database: 459 Effective search space: 204714 Effective search space used: 204714 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: 52 (24.6 bits)
This GapMind analysis is from Sep 24 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:
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