Align 1-pyrroline-5-carboxylate dehydrogenase 2; P5C dehydrogenase 2; EC 1.2.1.88; L-glutamate gamma-semialdehyde dehydrogenase (uncharacterized)
to candidate CCNA_02480 CCNA_02480 NAD-dependent benzaldehyde dehydrogenase II
Query= curated2:Q9K5Z5 (515 letters) >FitnessBrowser__Caulo:CCNA_02480 Length = 487 Score = 228 bits (582), Expect = 3e-64 Identities = 144/451 (31%), Positives = 226/451 (50%), Gaps = 16/451 (3%) Query: 52 IVSVNPAMKEQVIGVVSKASREIVDDAFKSAETAFHTWKNVNPEERANILIRAAAIIRRR 111 +++V E V+ V +A R V A SA+ A W + + R IL+RAA ++ Sbjct: 27 VIAVQEPATETVLTQVGRADRSDVARAAASAKAAQPAWAALTADARQAILLRAADLLVEH 86 Query: 112 KHEFSAWLVKEAGKPWKEADADTAEAIDFLEYYARQMITLKDGKPVNSREGEHNRYFYTP 171 + + W+++E+G +A + A F+ A M T G + S G+ + P Sbjct: 87 APDLAPWIMRESGSVAAKAAVELEHAAGFVRQ-AGAMATEAAGLVLPSSPGKTSIARRVP 145 Query: 172 IGVCVTISPWNFALAIMAGTTVAPIVTGNTVLLKPASTTPVVAAKFV-EVLEEAGLPKGV 230 +GV ISP+NF L + + TGN V+LKP TP+ + V E AGLP G+ Sbjct: 146 LGVVAVISPFNFPLVLSIRAVAPALATGNAVVLKPDPRTPISGGFLIARVFEAAGLPAGL 205 Query: 231 VNFVPGSGTDIGDYLIDHPKTSLITFTGSRDVGVRLYERAAVVHPGQQHLKRVIVEMGGK 290 ++ +PG + GD L P +++ FTGS G ++ E A HLK+V +E+GGK Sbjct: 206 LHVLPGDA-EAGDALCRDPNIAMVAFTGSTGAGRKVGEVAGA------HLKKVALELGGK 258 Query: 291 DTVVVDKDADLDLAAQSIVTSAFGFSGQKCSAGSRAVIHQDVYDVVLEKAVALTKQLSVG 350 + +++ DAD D+AA + A+ GQ C R ++ + ++D V+E+ A L VG Sbjct: 259 NPLIILDDADPDVAASNAAWGAWLHQGQVCMTAGRLLVQRGIHDAVVERLAAKAGHLPVG 318 Query: 351 EPTAPDVYMGPVVDQGAFSKIMSYIEVGKEEG-RLMVGGEGDDSKGFFIQPTIFADVDPH 409 +P DV +GP++ +G ++ + + +G RL+ GG KG PT+ V P Sbjct: 319 DPMRGDVALGPLISRGQLDRVHAIVSDTVADGARLVAGG---THKGLCYAPTVLTGVAPG 375 Query: 410 ARIMQEEIFGPVVAFSKARDFDHALEIANNTEYGLTGAVITTNRHHIEKAKRDFHVGNLY 469 R +EEIFGP+ A + D D A +AN+ YGL+ +I+ + VG+L+ Sbjct: 376 MRAFEEEIFGPIAAVTVFDDLDEAARLANDGPYGLSAGIISGSVGRAMTLGAKLEVGHLH 435 Query: 470 FNRNCTGAIVGYH-PFGGFKMSGTDSKAGGP 499 N A G H PFGG K SG ++ GP Sbjct: 436 INDQTVDA--GPHSPFGGMKASGNGTRISGP 464 Lambda K H 0.318 0.135 0.394 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: 606 Number of extensions: 27 Number of successful extensions: 7 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: 515 Length of database: 487 Length adjustment: 34 Effective length of query: 481 Effective length of database: 453 Effective search space: 217893 Effective search space used: 217893 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 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