Align 1-pyrroline-5-carboxylate dehydrogenase 2; P5C dehydrogenase 2; L-glutamate gamma-semialdehyde dehydrogenase; EC 1.2.1.88 (characterized)
to candidate WP_090218146.1 CV091_RS11005 aldehyde dehydrogenase
Query= SwissProt::P94391 (515 letters) >NCBI__GCF_002796795.1:WP_090218146.1 Length = 478 Score = 254 bits (650), Expect = 4e-72 Identities = 168/478 (35%), Positives = 263/478 (55%), Gaps = 25/478 (5%) Query: 41 INGERVETEAK--IVSINPADKEEVVGRVSKASQEHAEQAIQAAAKAFEEWRYTSPEERA 98 ING V+T+A+ I +NPA V+ + + S E AI AA A + W +P ERA Sbjct: 9 INGGFVDTKAQGIIPVLNPATGA-VLSEIPETSPEAVADAIAAAKTAQKGWEAKAPIERA 67 Query: 99 AVLFRAAAKVRRRKHEFSALLVKEAGKPWNEADAD---TAEAIDFMEYYARQMIELAKGK 155 L + +AK+R+ + +V E GK A+ + TA+ ID+M +AR++ +G+ Sbjct: 68 GYLRQISAKIRQNVPALAKTIVAEQGKTMGLAEVEVNFTADYIDYMAEWARRL----EGE 123 Query: 156 PVNSREGEKNQYVYTPT-GVTVVIPPWNFLFAIMAGTTVAPIVTGNTVVLKPASATPVIA 214 V S ++ +++ GV I PWNF F ++A ++TGNT+VLKP+ TP A Sbjct: 124 IVTSDNPNESIFLFRQAIGVVGGILPWNFPFFLIARKLAPALLTGNTIVLKPSEETPNNA 183 Query: 215 AKFVEVLEESGLPKGVVNFVPGSGAEVGDYLVDHPKTSLITFTGSREVGTRIFERAAKVQ 274 A F+++L E+ +PKGVVN V G GA G L ++P L++FTGS E G+RI AAK Sbjct: 184 AMFMDLLAETDMPKGVVNMVYGRGAVAGAALCENPDVGLLSFTGSVETGSRIMGAAAK-- 241 Query: 275 PGQQHLKRVIAEMGGKDTVVVDEDADIELAAQSIFTSAFGFAGQKCSAGSRAVVHEKVYD 334 ++ +V E+GGK +V +DAD++LAA++I S +GQ C+ R V V D Sbjct: 242 ----NITKVNLELGGKAPAIVLKDADLDLAAEAIVASRVINSGQVCNCAERVYVEASVED 297 Query: 335 QVLERVIE-ITESKVTAKPDSADVYMGPVIDQGSYDKIMSYIEIGKQEG-RLVSGG-TGD 391 +++ ++ + ++E K + V GP+I++ DK+ ++ K G +V+GG D Sbjct: 298 ELVAKLSQKMSEQKFGNPAEDFSVAYGPMINKAGLDKVAGMVDRAKAVGASVVTGGEVAD 357 Query: 392 DSKGYFIKPTIFADLDPKARLMQEEIFGPVVAFCKVSDFDEALEVANNTEYGLTGAVITN 451 +G + +PTI + +MQ+E+FGPV+ V D DEA+ AN++E+GLT ++ T Sbjct: 358 LGQGNYFQPTILTGCAQDSEIMQKEVFGPVLPVNAVKDIDEAITRANDSEFGLTSSIYTR 417 Query: 452 NRKHIERAKQEFHVGNLYFNRNCTGAIVGYHPFGGFKMS---GTDSKAGGPDYLALHM 506 + +A +E G Y NRN A+ GYH G + S G D K G ++ HM Sbjct: 418 DINSAMQACRELKFGETYINRNNFEAMQGYH--AGVRKSGIGGADGKHGLYEFTQTHM 473 Lambda K H 0.316 0.133 0.379 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: 576 Number of extensions: 29 Number of successful extensions: 5 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: 478 Length adjustment: 34 Effective length of query: 481 Effective length of database: 444 Effective search space: 213564 Effective search space used: 213564 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