GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpO in Collinsella tanakaei YIT 12063

Align glycerol-3-phosphate oxidase; EC 1.1.3.21 (characterized)
to candidate WP_009140573.1 HMPREF9452_RS02725 NAD(P)/FAD-dependent oxidoreductase

Query= CharProtDB::CH_000554
         (387 letters)



>NCBI__GCF_000225705.1:WP_009140573.1
          Length = 479

 Score =  188 bits (478), Expect = 2e-52
 Identities = 115/373 (30%), Positives = 197/373 (52%), Gaps = 9/373 (2%)

Query: 7   DICIIGGGIIGASVARELAKFDKKIVVLEANPRLALETSSHNSGLVHGGFDPRPETLNAK 66
           DI I+G GI G ++AR+L+++D  I  +EA   +AL ++  N GLVH G+DP   T+ A 
Sbjct: 5   DIVIVGAGITGCAIARQLSRYDLAIACVEAGNDIALGSTKANGGLVHAGYDPAAGTVKAS 64

Query: 67  LNVLGKKRYEDWIKEMDFPYLRIDSTIVAFNDEEMKHVHMLYDRGLINGLDPKEMQVIDA 126
           +N  G   Y  W KE+ F + R  S ++ F+  + +H+  L + G  NG++  +M++I+ 
Sbjct: 65  VNARGCALYGRWAKELGFGFKRTGSMVLGFSPADREHLEKLLENGRANGVE--DMRIIED 122

Query: 127 KELQKREPNISKQAVGALVCNSSIAIDPVLLTTTLMRNAIKNGVELKVNSKVVDIKKVDN 186
            E+ + EP  SK+A  AL C S+  +DP  +      NA  NGVE   ++ V  I +  +
Sbjct: 123 DEIWEHEPRASKEATCALWCPSTGYVDPFEVAIAAAENAAANGVEFWRSAAVDAIDEHAD 182

Query: 187 IFEIKTAKDEIIQAEVVVNVAGHYADVIANMAGYGDFKLTTRRGEYRILDKSEAGIVNSV 246
            F + T+  + + A  +VN AG+    I+ MAG   F+L  R+G   +LD     ++   
Sbjct: 183 GFVLHTSAGD-LSASYLVNAAGNGCADISRMAGGEHFELVWRQGNIAVLDHEARPLM--P 239

Query: 247 VFMVPTIHGKGVIVAPMLDGRVMVGPT-ALDGVPKEETLLVTQQQYDNIGKIGKHLIPNI 305
           ++ +PT   KGVIV   + G  ++  T A+      +T        + +    + L+P++
Sbjct: 240 LYPIPTSVSKGVIVTGTVHGNTVITATAAIHEAGDNDTYAA---DVEELLSGARKLVPDL 296

Query: 306 NMDKTCTVYAGSRPIDIETNDFIIRPAKNDKKFINVAGMKSPAIASAPAIADMVCDLVKN 365
           +  +    +AG R +    NDF+I  +    +    AG++SP +ASAPA+A+ +  L++ 
Sbjct: 297 DTRRLVRAFAGGRAVIRGLNDFLIERSAAQPRLFQAAGIQSPGVASAPAVAERIEGLIRQ 356

Query: 366 AFDKLDKKANWQP 378
           A   L +K  + P
Sbjct: 357 AGITLIEKPGYNP 369


Lambda     K      H
   0.318    0.136    0.391 

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: 382
Number of extensions: 20
Number of successful extensions: 5
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: 387
Length of database: 479
Length adjustment: 32
Effective length of query: 355
Effective length of database: 447
Effective search space:   158685
Effective search space used:   158685
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: 51 (24.3 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