GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fahA in Sinorhizobium fredii NGR234

Align fumarylacetoacetate (FAA) hydrolase (EC 3.7.1.2) (characterized)
to candidate YP_002827492.1 NGR_c29960 aromatic amino acid degradation protein

Query= reanno::psRCH2:GFF3447
         (327 letters)



>NCBI__GCF_000018545.1:YP_002827492.1
          Length = 338

 Score =  423 bits (1087), Expect = e-123
 Identities = 220/336 (65%), Positives = 252/336 (75%), Gaps = 12/336 (3%)

Query: 1   MKLATLNQG-RDGVLVVVSRDLAQAVKVPQIAATLQAALDDWNYCKPKLEAVYQRLNDGL 59
           MKLATL    RDG LVVVSRDL +  +V  IA TLQ ALDDW +  P+L  V + +  G 
Sbjct: 1   MKLATLKDSTRDGKLVVVSRDLTRCSEVGHIARTLQTALDDWAHAGPRLARVAEGIETG- 59

Query: 60  EEGAFAFDQTACHSPLPRAYHWADGSAYVNHVELVRKARGAEMPESFWHDPLMYQGGADA 119
            +    F +    SPLPRA+HWADGSAYVNHVELVRKAR AEMP SFW DPL+YQGG+D+
Sbjct: 60  SQPTMRFHEHDAASPLPRAFHWADGSAYVNHVELVRKARDAEMPASFWTDPLIYQGGSDS 119

Query: 120 FIPPHSPIRLADEAWGIDLEGELAVITDDVPMGATPAEAASHIQLLMLVNDVSLRNLIPG 179
           F+ P  PI++ADEAWGIDLEGE+AVI DDVPMGAT  EA   I+L+MLVNDVSLR LIPG
Sbjct: 120 FVGPRDPIQVADEAWGIDLEGEVAVIVDDVPMGATVDEAREAIRLVMLVNDVSLRGLIPG 179

Query: 180 ELAKGFGFYQSKPSSSFSPVAVTPDELGETWRDGKVHRPLVSHINGELFGQPDAGTDMTF 239
           ELAKGFGFYQSKPSS+FSPV VTPDELG+ W  GK+H PL   +NG+ FG+ +AG DMTF
Sbjct: 180 ELAKGFGFYQSKPSSAFSPVGVTPDELGDAWDGGKMHLPLRVDLNGKPFGRANAGIDMTF 239

Query: 240 NFPTLVAHAARTRPLGAGTIIGSGTVSN----------YDRSAGSSCLAEKRMLEVVEHG 289
           +FP L+ HAARTRPL AGTIIGSGTVSN           D   G SC+AE RM+E +E G
Sbjct: 240 DFPQLIVHAARTRPLSAGTIIGSGTVSNKLDGGPGKPVSDGGVGYSCIAELRMIETIETG 299

Query: 290 EAKTPFLKFGDRVRIEMFDAAGQSIFGAIDQQVERY 325
            AKT FLKFGD VRIEM D  G SIFGAI+Q+VERY
Sbjct: 300 AAKTSFLKFGDVVRIEMKDKTGHSIFGAIEQKVERY 335


Lambda     K      H
   0.318    0.135    0.411 

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: 412
Number of extensions: 19
Number of successful extensions: 3
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: 327
Length of database: 338
Length adjustment: 28
Effective length of query: 299
Effective length of database: 310
Effective search space:    92690
Effective search space used:    92690
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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:

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:

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