GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Thiohalospira halophila HL 3

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate WP_093428323.1 BM272_RS08315 adenosylmethionine--8-amino-7-oxononanoate transaminase

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_900112605.1:WP_093428323.1
          Length = 449

 Score =  187 bits (476), Expect = 5e-52
 Identities = 116/344 (33%), Positives = 188/344 (54%), Gaps = 28/344 (8%)

Query: 76  LVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAK--QPLHSQELLDPLRAMLAKTL 133
           L D  G+EFID +  + +   GH NP + + ++ Q+ +    + +    +P+   L++ L
Sbjct: 40  LEDYDGREFIDAVSSWWVNLFGHANPRINARIREQMEQLEHVILAGFSHEPV-VELSERL 98

Query: 134 AALTPGKLKYSFFCNSGTESVEAALKLAKAYQSPRG---KFTFIATSGAFHGKSLGALSA 190
             L P  L  +F+ ++G+ ++E ALK++  Y   RG   K  F+A +G++HG++LGALS 
Sbjct: 99  VDLAPEGLTRAFYADNGSSAIEVALKMSFHYWLNRGQSQKTRFVALTGSYHGETLGALSV 158

Query: 191 TAKSTFRKPFMPLLPGFRHVPFGNI----------EAMRTALNECKK----TGDDVAAVI 236
                +R+ + PLL    H P  +           E       E ++      D+V AV+
Sbjct: 159 GHVPLYRETYGPLLLEAIHAPSPDCYHREPGEDCAEYAERQFAEMERILAENADEVCAVV 218

Query: 237 LEP-IQGEGGVILPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDI 295
           +EP +Q  GG+ +  P YL  +R+ CD +G  +I DE+  G GRTG MFACE   + PD 
Sbjct: 219 VEPLVQCVGGMRMHDPVYLERLREACDRYGIHLIADEIAVGFGRTGTMFACEQAGITPDF 278

Query: 296 LCLAKALGGGVMPIGATIATEEVFSVLFDN-----PFLHTTTFGGNPLACAAALATINVL 350
           +CL+K L  G +P+ AT+ TEEV+   +D+      FLH+ +F GNPL CAAALAT+++ 
Sbjct: 279 MCLSKGLTAGYLPLAATLTTEEVYCAFYDDFNNLTAFLHSHSFTGNPLGCAAALATLDIF 338

Query: 351 LEQNLPAQAEQKGDMLLDGFRQLAREYPDLVQEARGKGMLMAIE 394
            E  +     +K +++ +    L  ++P  V E R  GM++A E
Sbjct: 339 AEDEVIESNRRKAEVMGEAMAPL-NDHPK-VAEVRQTGMILAAE 380


Lambda     K      H
   0.320    0.135    0.393 

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: 476
Number of extensions: 22
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: 459
Length of database: 449
Length adjustment: 33
Effective length of query: 426
Effective length of database: 416
Effective search space:   177216
Effective search space used:   177216
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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