GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Methylocapsa acidiphila B2

Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate WP_026608078.1 METAC_RS0117865 alpha-hydroxy-acid oxidizing protein

Query= reanno::WCS417:GFF3737
         (376 letters)



>NCBI__GCF_000427445.1:WP_026608078.1
          Length = 376

 Score =  569 bits (1466), Expect = e-167
 Identities = 280/375 (74%), Positives = 317/375 (84%)

Query: 1   MIISSASDYRAAAKRKLPRFLFDYIDGGAYAEHTLRANSSDLAEISLRQRILRNVDNLSL 60
           MI+SSASDYR AA+R LP FLFDYIDGGA AE TL+AN +DLAE+ LRQR+L+NV +LSL
Sbjct: 1   MIVSSASDYREAARRGLPSFLFDYIDGGANAEQTLKANMADLAEVILRQRVLKNVSDLSL 60

Query: 61  KTTLFGQELDMPVILSPVGLTGMYARRGEVQAAKAAANKGIPFCLSTVSVCPIEEVASQS 120
            T  FGQ   +P+IL PVGL GM ARRGEVQ AKAAA KG+PF LSTVSVC +EEVASQ 
Sbjct: 61  ATEWFGQPSALPLILGPVGLAGMLARRGEVQVAKAAAKKGVPFVLSTVSVCSLEEVASQC 120

Query: 121 AQAIWFQLYVLKDRGFMRNALERAQAAGVTTLVFTVDMPTPGARYRDAHSGMSGPFAAQR 180
            + IWFQLYVLKDRGFMRN LERA+AAGV  LVFTVDM  PGARYRDAHSGMSGPFAAQR
Sbjct: 121 PRPIWFQLYVLKDRGFMRNVLERAEAAGVKNLVFTVDMAVPGARYRDAHSGMSGPFAAQR 180

Query: 181 RMLQAVTKPQWAFDVGLMGRPHDLGNISKYLGKPTHLEDYIGWLANNFDASISWKDLEWI 240
           R+LQA+TKP WAFDVGL GRPHDLGN+S Y G+   L DY+GW+  NFD SI W DLEWI
Sbjct: 181 RILQAITKPAWAFDVGLRGRPHDLGNVSSYFGEAIALSDYMGWIGKNFDPSICWADLEWI 240

Query: 241 REFWKGPMIIKGILDPQDAKDAVSFGADGIVVSNHGGRQLDGVLSTAKALPPIADAVGDD 300
           R+FWKGPMIIKGILD +DA+DA+ FGA+GIVVSNHGGRQLDG LSTAKALPPI DAVG D
Sbjct: 241 RDFWKGPMIIKGILDSEDARDAIRFGANGIVVSNHGGRQLDGALSTAKALPPIVDAVGSD 300

Query: 301 LTVLVDSGIRSGLDVVRMLALGAKACLLGRATAYALAADGQHGVENLLDIFAKEMRVAMT 360
           L VL DSG+RSGLDVVRMLALGAK  +LGR  A+ALAA+GQ GVEN+LDIFA E+R+AMT
Sbjct: 301 LVVLADSGVRSGLDVVRMLALGAKGVMLGRVPAFALAANGQAGVENVLDIFANEIRIAMT 360

Query: 361 LTGVTSIAQIDRSTL 375
           L GV S++QI+++ L
Sbjct: 361 LIGVPSVSQINKTVL 375


Lambda     K      H
   0.321    0.136    0.401 

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: 490
Number of extensions: 14
Number of successful extensions: 1
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: 376
Length of database: 376
Length adjustment: 30
Effective length of query: 346
Effective length of database: 346
Effective search space:   119716
Effective search space used:   119716
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 (21.9 bits)
S2: 50 (23.9 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