GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galT in Malonomonas rubra DSM 5091

Align galactose-1-phosphate uridylyltransferase (EC 2.7.7.12) (characterized)
to candidate WP_072908934.1 BUB13_RS11630 galactose-1-phosphate uridylyltransferase

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



>NCBI__GCF_900142125.1:WP_072908934.1
          Length = 348

 Score =  224 bits (572), Expect = 2e-63
 Identities = 126/352 (35%), Positives = 190/352 (53%), Gaps = 28/352 (7%)

Query: 11  ELRKDSVTNRWVIFSPARAKRPSDFKSKSPAPSSTDSPQTCPFCIGQEHHCAPEIFRFPP 70
           ELR D + N W I +  R +RP DF  K            CPFC G E    PEI+ + P
Sbjct: 3   ELRWDPLKNNWTIMTKGRGRRPQDFLQKREQVKMA----ACPFCNGNETKTPPEIYAYRP 58

Query: 71  QN-----PDWKVRVIQNLYPALSRDKDLDSSTSLSSGSLLWGCLLDGYGFHDVIIESPVH 125
                  P W+VRVI N +PAL  + +LD+        +      +G G H+VIIE P H
Sbjct: 59  DGSRANQPGWQVRVIPNKFPALGIEGELDNRAEGLYDRM------NGIGAHEVIIEHPDH 112

Query: 126 SVHLSDLTPEDVAQVLFAYKKRILQLASDDSIKYVQVFKNHGASAGASMTHPHSQMVGLP 185
              ++DLT +++A+VL AY+ R+L L  D   +Y+ VFKN G  A A++ H HSQ++ +P
Sbjct: 113 DKSMADLTTDELAEVLKAYRARMLDLHRDGRFRYIFVFKNFGIEAAANVPHSHSQLIAVP 172

Query: 186 VIPPSVTTRLDSMKQYFNETGKCSICHV-----PTKDLLVDESVHFISVVPYAASFPFEL 240
           ++PP + T L+S +++F    +C IC +      TK  +V +  +FIS  PYA+ FPFEL
Sbjct: 173 LVPPLIATELESCREHFARKERCLICDLIRQERETKTRVVRDDGNFISYAPYASKFPFEL 232

Query: 241 WIVPRDHVSHFHELDQEKAVDLGGLLKVTLIKMSLQLNKPPFNFMIHTSP---LQASDSD 297
            I P  H   F     ++ + L   L  +L ++   L  PP++F++H +P   L+    D
Sbjct: 233 MIAPLQHSHDFTLCTDQQLLLLADTLGDSLRRLRSILRDPPYSFILHNAPPLHLRRGRPD 292

Query: 298 LAYS-----HWFFQIVPHLSGVGGFELGTGCYINPVFPEDAAKVMREVNISI 344
              S     HW  +I P L+ V GFE G+G  +NP  PE+AA+ +R+ + ++
Sbjct: 293 YWGSLPVDYHWHIEIAPKLTNVAGFEWGSGFQMNPTPPEEAAEFLRQADPTV 344


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: 317
Number of extensions: 17
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: 348
Length adjustment: 29
Effective length of query: 315
Effective length of database: 319
Effective search space:   100485
Effective search space used:   100485
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