Align N-succinylglutamate 5-semialdehyde dehydrogenase 1; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase 1; SGSD 1 (uncharacterized)
to candidate WP_111608696.1 DK187_RS17920 betaine-aldehyde dehydrogenase
Query= curated2:Q12QD2 (498 letters) >NCBI__GCF_003259225.1:WP_111608696.1 Length = 485 Score = 207 bits (528), Expect = 5e-58 Identities = 159/460 (34%), Positives = 231/460 (50%), Gaps = 19/460 (4%) Query: 12 QTQFIAGQWLAG-KGPSFSSVNPANGEVIWQGLGADAGQVDAAITSARAAFYTWSAMSLT 70 Q Q+I G++ A G F ++NPA GEVI A ++DAA+ SA+ W+AMS Sbjct: 4 QQQYIHGRYHASTSGEHFETINPATGEVIATVEHAGQAELDAAVESAKQGQKVWAAMSPV 63 Query: 71 ERLVIVEAFAEQLKEHAELFARTIALETGKALWESRTEVGAMTGKIAISIKANA--ERTG 128 ER I++ AE L+E+ E AR L+TGK L E+ V TG I A + G Sbjct: 64 ERGRILKKAAELLRENNEELARLEVLDTGKPLQEAIC-VDIQTGADVIEYYAGLTDKIQG 122 Query: 129 TVENPMPGAKAFIRHKPHGVVAVFGPYNFPGHLPNGHIVPALIAGNTVLFKPSELTPKVA 188 ++ G + R +P G+ A G +N+P + PAL AGN ++FKPSE TP A Sbjct: 123 DYQDLGNGNFFYTRREPLGICAGIGAWNYPIQIAMWKSGPALAAGNAMIFKPSEETPLTA 182 Query: 189 ELTMQLWQQAGLPNGVLNLLQGEIATGKALASHKGIDGLFFTGSSNTGHLLHQQYAGQPG 248 +++ QAGLP+GV N++QG+ TG+ + +H I + FTG TG + + Q Sbjct: 183 LKLAEIFTQAGLPDGVFNVIQGDGRTGQMITAHPDIAKVSFTGEVGTGKKV-MAASAQSL 241 Query: 249 KILALEMGGNNPLIITEVANVDAAVHDIIQSAFISSGQRCTCARRLFIPKTANGDAILAK 308 K + +E+GG +P+II VD AV + + F + G+ CT R+F+ DA + Sbjct: 242 KQVTMELGGKSPMIIFPDMPVDQAVSAAMLANFYTQGEVCTNGTRVFVHADML-DAFTKE 300 Query: 309 LLTSTAKIALGDPFAETQPFFGAMISD---KAAAGMVKAQADIQAAGGVSLIELTQVT-P 364 L T + +GDP + GA+IS + G ++A D AG L QVT Sbjct: 301 LKARTEAMIIGDPM-DMNTQVGALISKDHMQKVLGYIQAAKD---AGATLLCGGYQVTEK 356 Query: 365 GL---GFVTPGII-DVTDASPLADEEHFGPLLKVYRYTDFDAAIDEANNTSFGLSAGLLA 420 GL FV P + D TD P +E FGP++ V +TD D I AN+T GL+AG+ Sbjct: 357 GLDKGAFVAPTVFTDCTDDMPQVRDEIFGPVMSVLSFTDEDEVIARANDTKLGLAAGVFT 416 Query: 421 DSETDYQHFYRRIRAGIVNWNKPITGASSAAPFGGIGASG 460 +++AGI W + + P GG SG Sbjct: 417 KDFARAHRVINQLQAGIC-WINAWGASPAEMPVGGYKESG 455 Lambda K H 0.317 0.133 0.390 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: 558 Number of extensions: 32 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: 498 Length of database: 485 Length adjustment: 34 Effective length of query: 464 Effective length of database: 451 Effective search space: 209264 Effective search space used: 209264 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 (21.7 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