GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galT in Ammonifex degensii KC4

Align galactose-1-phosphate uridylyltransferase (EC 2.7.7.12) (characterized)
to candidate WP_015738480.1 ADEG_RS02275 galactose-1-phosphate uridylyltransferase

Query= metacyc::MONOMER-15710
         (344 letters)



>NCBI__GCF_000024605.1:WP_015738480.1
          Length = 341

 Score =  260 bits (665), Expect = 3e-74
 Identities = 136/343 (39%), Positives = 199/343 (58%), Gaps = 22/343 (6%)

Query: 10  PELRKDSVTNRWVIFSPARAKRPSDFKSKSPAPSSTDSPQTCPFCIGQEHHCAPEI--FR 67
           PE RKD V +RWV  S  RAKRP+D++     P      + CP C+G E    PE+  FR
Sbjct: 2   PEWRKDPVVDRWVAVSTERAKRPTDYRP----PLERKKQERCPLCVGHEGDTPPEVMAFR 57

Query: 68  FP---PQNPDWKVRVIQNLYPALSRDKDLDSSTSLSSGSLLWGCLLDGYGFHDVIIESPV 124
            P   P +P W VRV+ N +PA   +++         G   W C   G G H+VI+E+P 
Sbjct: 58  HPGSLPDHPGWWVRVVPNKFPACRVEEE---DIVRPHGPYQWRC---GVGAHEVIVETPE 111

Query: 125 HSVHLSDLTPEDVAQVLFAYKKRILQLASDDSIKYVQVFKNHGASAGASMTHPHSQMVGL 184
           H  +L + +   +A+V++A++ R+L L  D   KY+Q+FKN G+ AGAS+ H HSQ++ L
Sbjct: 112 HVPNLVNQSEGQIAEVIWAWRARLLDLRRDTRFKYIQIFKNKGSVAGASLEHTHSQLIAL 171

Query: 185 PVIPPSVTTRLDSMKQYFNETGKCSICHVPTKDL-----LVDESVHFISVVPYAASFPFE 239
           P++P  +   L  +K Y  E G C  C +   +L     +V+ES HF+  VPYAA FPFE
Sbjct: 172 PMVPAEIQAELTGVKVYREEKGSCVFCDLWRYELEAGERVVEESSHFLCFVPYAARFPFE 231

Query: 240 LWIVPRDHVSHFHELDQEKAVDLGGLLKVTLIKMSLQLNKPPFNFMIHTSPLQASDSDLA 299
           +W+VP+ H   F  +++ +  DL  LLK TL +++  +  PPFN ++HT+P+   +    
Sbjct: 232 MWLVPKRHKPDFGAIEEGEVCDLAWLLKRTLYRLAQTVFDPPFNLVLHTAPVNVPEP--V 289

Query: 300 YSHWFFQIVPHLSGVGGFELGTGCYINPVFPEDAAKVMREVNI 342
             HW  +I+P L+ + GFELGTG YINP  PE AA  +RE  +
Sbjct: 290 DYHWHIEILPRLTIMAGFELGTGYYINPTPPEMAAAALREQEV 332


Lambda     K      H
   0.320    0.135    0.421 

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: 400
Number of extensions: 19
Number of successful extensions: 6
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: 344
Length of database: 341
Length adjustment: 29
Effective length of query: 315
Effective length of database: 312
Effective search space:    98280
Effective search space used:    98280
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 (21.8 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