GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Sulfuricurvum kujiense DSM 16994

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate WP_013450014.1 SULKU_RS13855 aspartate aminotransferase family protein

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_000183725.1:WP_013450014.1
          Length = 388

 Score =  166 bits (421), Expect = 9e-46
 Identities = 120/373 (32%), Positives = 192/373 (51%), Gaps = 25/373 (6%)

Query: 68  WQAGSLNTLVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQEL--LDPL 125
           ++ G   TL D++G+E+ID   G  + +VGH N  +  A+ +Q AK  LH   L  ++P 
Sbjct: 17  FERGDNATLCDSEGKEYIDFAAGVAVCSVGHGNCRLARAISDQAAKI-LHVSNLYRIEP- 74

Query: 126 RAMLAKTLAALTPGKLKYSFFCNSGTESVEAALKLAKAYQSPRG---KFTFIATSGAFHG 182
           +   A+ +  L+   ++  FF NSGTE+ E A+K+A+ Y    G   ++  I    +FHG
Sbjct: 75  QEECARRIVELSGYDMR-CFFGNSGTEANEGAIKIARKYGERDGSIKRYKIITLENSFHG 133

Query: 183 KSLGALSATAKSTFRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQG 242
           +++ AL AT +++    F P   GF +    N+E + + ++E         AV++E +QG
Sbjct: 134 RTITALKATGQASKHDYFGPYPDGFVYA--ANVEEIESLIDET------TVAVMIELVQG 185

Query: 243 EGGVILPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKAL 302
           EGGV       +  +  L      L+I+DEVQTG+ R G   A  +  + PD++ LAK L
Sbjct: 186 EGGVQPLDKQKVQNLSALLKSKDILLIVDEVQTGIYRCGSFLASHYYGITPDVITLAKGL 245

Query: 303 GGGVMPIGATIA-TEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQ 361
           GGGV PIG  +   +E+FS        H +TFGGN L+  AA   +++L   N   +  +
Sbjct: 246 GGGV-PIGVVMTRLKEIFSY-----GDHGSTFGGNYLSTVAANEVLDILEAYNKSGEMME 299

Query: 362 KGDMLLDGFRQLAREYPDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRVLVAGTLNN 421
             +      +  A  YPD+  E  G GM+  +  +D+E+        F   VLV  +  N
Sbjct: 300 HQNYFETSLKSFALHYPDIFTERVGIGMMQGLRVIDSEVLSKIIDSAFEIGVLVIKSGRN 359

Query: 422 AKTIRIEPPLTLT 434
             T+R  PPLT++
Sbjct: 360 --TLRFVPPLTIS 370


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: 380
Number of extensions: 24
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: 388
Length adjustment: 32
Effective length of query: 427
Effective length of database: 356
Effective search space:   152012
Effective search space used:   152012
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: 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