GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Mycolicibacterium vanbaalenii PYR-1

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate WP_011778553.1 MVAN_RS06505 ornithine--oxo-acid transaminase

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_000015305.1:WP_011778553.1
          Length = 403

 Score =  214 bits (546), Expect = 3e-60
 Identities = 132/374 (35%), Positives = 198/374 (52%), Gaps = 25/374 (6%)

Query: 76  LVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLAKTLAA 135
           + D +G+ ++DCL  +   N GHRNP V++    QL    L S+       A     LA 
Sbjct: 39  ITDVEGRRYLDCLAAYSAVNFGHRNPEVIATAHAQLDAVTLVSRAFHSDRLAPFCAALAD 98

Query: 136 LTPGKLKYSFFCNSGTESVEAALKLAKAYQ-SPRGKFT--FIATSGAFHGKSLGALSATA 192
           L    +      NSG E+VE+ +K+A+ +    +G  T   +     FHG++   +S + 
Sbjct: 99  LCGKDMVLPM--NSGAEAVESGIKVARKWGVDVKGVKTPNIVVAHNNFHGRTTTIISFSD 156

Query: 193 KSTFRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVILPPPG 252
             T R+ F P  PGFR VPFG+ +A+  A++      DD  AV++EPIQGE G+I+PP  
Sbjct: 157 DETARRGFGPYTPGFRSVPFGDADALAPAVD------DDTVAVLIEPIQGEAGIIVPPDD 210

Query: 253 YLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVMPIGAT 312
           YL  VR LC E   LMI DE+Q+G+ RTG+ FAC+H  V PDI  L KALGGGV+P+ A 
Sbjct: 211 YLPRVRALCTERNVLMIADEIQSGLARTGRTFACDHWGVVPDIYLLGKALGGGVLPLSAV 270

Query: 313 IATEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDML---LDG 369
           +A  ++  VL  +P  H +TFGGNPLA A     +++L       ++ + G  L   L+G
Sbjct: 271 VADRDILGVL--HPGEHGSTFGGNPLAAAIGSTVVDILRRGEFQRRSTELGAHLHARLNG 328

Query: 370 FRQLAREYPDLVQEARGKGMLMAIEF-VDNEIGYNFASEMFRQRVLVAGTLNNAKTIRIE 428
            +         V   RG+G+   ++    +  G   +  +  + VLV  T  +  T+R  
Sbjct: 329 LKGRG------VLAVRGRGLWAGVDIDPAHGTGKQVSLRLAERGVLVKDT--HGSTLRFA 380

Query: 429 PPLTLTIEQCELVI 442
           PPL +T ++ +  I
Sbjct: 381 PPLVITADEIDWAI 394


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: 410
Number of extensions: 15
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: 403
Length adjustment: 32
Effective length of query: 427
Effective length of database: 371
Effective search space:   158417
Effective search space used:   158417
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