GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Beijerinckia indica ATCC 9039

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate WP_012385734.1 BIND_RS14190 ornithine--oxo-acid transaminase

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_000019845.1:WP_012385734.1
          Length = 412

 Score =  228 bits (581), Expect = 3e-64
 Identities = 142/366 (38%), Positives = 205/366 (56%), Gaps = 23/366 (6%)

Query: 76  LVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLAKTLAA 135
           L D  G+ ++D +  +   + GH +P +V A++ QL +  L S+           + LA 
Sbjct: 32  LFDCDGRRYLDMMSAYSAASFGHLHPRLVGALKRQLERLDLVSRAYHTDTLGPFCEDLAR 91

Query: 136 LTPGKLKYSFFCNSGTESVEAALKLAKAY-----QSPRGKFTFIATSGAFHGKSLGALSA 190
           LT   L      N+G E+VE A+K A+ Y       P  +   I  +G FHG++   +  
Sbjct: 92  LTG--LDACLPMNTGAEAVETAIKAARRYGYDRLSIPEDQAEIIVAAGNFHGRTTTIIGF 149

Query: 191 TAKSTFRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVILPP 250
           ++ +  R+ F P  PGF  VPFG+  A+  A+      G   AAV++EPIQGE G+ILPP
Sbjct: 150 SSDAATRRGFGPFAPGFVLVPFGDAGALEAAV------GPRTAAVLIEPIQGEAGIILPP 203

Query: 251 PGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVMPIG 310
           PGYL A+R+LCD  G L+I DEVQ+G GRTG+ FA EHE  +PD L L KALGGG++P+ 
Sbjct: 204 PGYLAALRRLCDRHGILLIFDEVQSGFGRTGRTFAFEHEGAKPDGLILGKALGGGLLPVS 263

Query: 311 ATIATEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDMLLDGF 370
           A  A   +  V   +P  H +TFGGNPLA A A   ++VL E++L  ++E+ G +LLD  
Sbjct: 264 AFAAKRSLMDVF--DPGSHGSTFGGNPLAMAVAREAMHVLQEEHLVERSEKLGGVLLDAL 321

Query: 371 RQLAREYPDLVQEARGKGMLMAIEFVDNEI--GYNFASEMFRQRVLVAGTLNNAKTIRIE 428
           R  A ++P  V   RGKG+   ++ +D  +        +M  + VL   T  +A TIR  
Sbjct: 322 R--AIDHP-AVLAVRGKGLWAGVD-LDPALADAKKVCLKMMERGVLTKET--HATTIRFA 375

Query: 429 PPLTLT 434
           PPL +T
Sbjct: 376 PPLVIT 381


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: 457
Number of extensions: 40
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: 459
Length of database: 412
Length adjustment: 32
Effective length of query: 427
Effective length of database: 380
Effective search space:   162260
Effective search space used:   162260
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.

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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