Alignments for a candidate for xacF in Rhodobacter viridis JA737

GapMind for catabolism of small carbon sources

Alignments for a candidate for xacF in Rhodobacter viridis JA737

Align Alpha-ketoglutaric semialdehyde dehydrogenase 1; alphaKGSA dehydrogenase 1; 2,5-dioxovalerate dehydrogenase 1; 2-oxoglutarate semialdehyde dehydrogenase 1; KGSADH-I; Succinate-semialdehyde dehydrogenase [NAD(+)]; SSDH; EC 1.2.1.26; EC 1.2.1.24 (characterized)
to candidate WP_110804869.1 C8J30_RS06315 NAD-dependent succinate-semialdehyde dehydrogenase

Query= SwissProt::Q1JUP4
         (481 letters)



>NCBI__GCF_003217355.1:WP_110804869.1
          Length = 492

 Score =  324 bits (830), Expect = 5e-93
 Identities = 184/469 (39%), Positives = 250/469 (53%), Gaps = 1/469 (0%)

Query: 9   TQLLIDGEWVDAASGKTIDVVNPATGKPIGRVAHAGIADLDRALAAAQSGFEAWRKVPAH 68
           T+ L+ GEWVDA  GKT  V+NPA G  I  V     AD  RA+ AA+   + W      
Sbjct: 20  TKALVAGEWVDAEDGKTFAVMNPARGDVICTVPDLTRADTARAIKAAEVAMKDWAARTGK 79

Query: 69  ERAATMRKAAALVRERADAIAQLMTQEQGKPLTEARVEVLSAADIIEWFADEGRRVYGRI 128
           ERAA MRK   L+    + +A ++T E GKPL EAR E+   A  IEWF +E +R+YG  
Sbjct: 80  ERAAVMRKWFELMMANQEDLALILTAEMGKPLAEARGEIAYGASFIEWFGEEAKRIYGET 139

Query: 129 VPPRNLGAQQTVVKEPVGPVAAFTPWNFPVNQVVRKLSAALATGCSFLVKAPEETPASPA 188
           +P      + TV+K+P+G V + TPWNFP   + RK   A+A GC F+ +   ETP S  
Sbjct: 140 IPGHMRDKRITVLKQPIGVVGSITPWNFPNAMIARKAGPAIAVGCGFVCRPASETPLSAL 199

Query: 189 ALLRAFVDAGVPAGVIGLVYGDPA-EISSYLIPHPVIRKVTFTGSTPVGKQLASLAGLHM 247
           A+      AG+P G++ ++    A +I      +  +RK+TFTGST VG+ L   A   +
Sbjct: 200 AMGLLGERAGLPKGILSVITSSRASDIGKEFCENHAVRKLTFTGSTEVGRILLRQAADQV 259

Query: 248 KRATMELGGHAPVIVAEDADVALAVKAAGGAKFRNAGQVCISPTRFLVHNSIRDEFTRAL 307
            + +MELGG+AP IV +DAD+  AV+ A  +KFRN GQ C+   R  V   + D F   L
Sbjct: 260 MKCSMELGGNAPFIVFDDADLDAAVEGAMMSKFRNNGQTCVCANRIYVQAGVYDTFAEKL 319

Query: 308 VKHAEGLKVGNGLEEGTTLGALANPRRLTAMASVIDNARKVGASIETGGERIGSEGNFFA 367
                 L VG+GL++G T G L +   +  +   I +    G +I TGG R    G FF 
Sbjct: 320 AAAVRKLNVGDGLKDGVTTGPLISADAVEKVEEHIADVVAGGGTIVTGGARHELGGTFFQ 379

Query: 368 PTVIANVPLDADVFNNEPFGPVAAIRGFDKLEEAIAEANRLPFGLAGYAFTRSFANVHLL 427
           PTV+  V     V   E FGPVA +  F+   E I +AN   FGLA Y + R    +  +
Sbjct: 380 PTVVTGVTQAMKVATEETFGPVAPLFKFETEAEVIEKANATIFGLASYFYARDVGRITRV 439

Query: 428 TQRLEVGMLWINQPATPWPEMPFGGVKDSGYGSEGGPEALEPYLVTKSV 476
            + LE G++ +N         PFGGVK SG G EG    +E YL  K V
Sbjct: 440 QEGLEYGIVGVNTGIISTEVAPFGGVKQSGLGREGSHHGVEDYLELKYV 488


Lambda     K      H
   0.318    0.134    0.393 

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: 598
Number of extensions: 19
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: 481
Length of database: 492
Length adjustment: 34
Effective length of query: 447
Effective length of database: 458
Effective search space:   204726
Effective search space used:   204726
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.

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Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
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About GapMind

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources