GapMind for catabolism of small carbon sources

 

Alignments for a candidate for antC in Marinobacter adhaerens HP15

Align Anthranilate 1,2-dioxygenase electron transfer component; EC 1.18.1.3 (characterized)
to candidate GFF1129 HP15_1107 oxidoreductase FAD/NAD(P)-binding domain protein

Query= SwissProt::O85675
         (343 letters)



>FitnessBrowser__Marino:GFF1129
          Length = 338

 Score =  269 bits (687), Expect = 9e-77
 Identities = 134/334 (40%), Positives = 208/334 (62%), Gaps = 2/334 (0%)

Query: 3   HSVALNFADGKTFFIAVQEDELLLDAAVRQGINLPLDCREGVCGTCQGTCETGIYEQEYV 62
           + VALNF DG T FI     E + +AA R GIN+PLDCR+G CGTC+  CE+G YE E  
Sbjct: 2   YKVALNFEDGITRFITTSPMETVANAAYRSGINIPLDCRDGACGTCKCHCESGTYEMEGF 61

Query: 63  DEDALSERDLAKRKMLACQTRVKSNAAFYFDHHSSICNAGETLKIATVVTGVELVSETTA 122
            EDALS+ ++    +L CQ   +S+        S +C  G    I   ++ V+ +S T A
Sbjct: 62  IEDALSDEEVRLGYVLTCQMIPESDCVVTVPASSEVCLKGGASDIFAELSEVKQLSRT-A 120

Query: 123 ILHLDASQHVKQLDFLPGQYARLQIPDTDDWRSYSFANRPNASNQL-QFLIRLLPNGVMS 181
           +  + + + V+ + FLPGQYA++Q+P TD++R+YSF++  N +N L  FL+R++P G+MS
Sbjct: 121 LSFVVSGEGVRAMQFLPGQYAKIQVPGTDEFRAYSFSSMVNHANGLVSFLMRVVPEGLMS 180

Query: 182 NYLRERCQVGQTLIMEAPLGSFYLREVERPLVFIAGGTGLSAFLGMLDNIAEQPNQPSVH 241
            Y+  +  VG ++ +  P GSFYLREV+RP++ +AGGTGL+ FL ML+ I  + +   +H
Sbjct: 181 GYMTHKSSVGDSIALRGPFGSFYLREVKRPVLMLAGGTGLAPFLAMLEKIQLEGSDYPIH 240

Query: 242 LYYGVNTEADLCEQKRLTTYAERIKNFSYHPIISKASEQWQGKSGFIHEHLDKNQLSEQS 301
           + YGV  E DL    +L  +AE I NF++   ++ +      + G++  H++   L++ +
Sbjct: 241 MVYGVTHEVDLVALDQLEAFAEAIGNFTFSACVASSECGSWPQKGYVTHHIEPEHLNDGN 300

Query: 302 FDMYLCGPPPMIEAVKTWLDEQAIADCHIYSEKF 335
            D+YLCGPPPM++AV +++ E+ I     Y EKF
Sbjct: 301 VDIYLCGPPPMVDAVSSFIQEKGIQPVSFYYEKF 334


Lambda     K      H
   0.319    0.134    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: 304
Number of extensions: 9
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: 343
Length of database: 338
Length adjustment: 28
Effective length of query: 315
Effective length of database: 310
Effective search space:    97650
Effective search space used:    97650
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 17 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