GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Trichormus variabilis ATCC 29413

Align NatD, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized)
to candidate WP_011317349.1 AVA_RS02360 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_000204075.1:WP_011317349.1
          Length = 316

 Score =  138 bits (347), Expect = 2e-37
 Identities = 100/313 (31%), Positives = 169/313 (53%), Gaps = 36/313 (11%)

Query: 1   MDIQT-IQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFV--NTF 57
           MDI   +Q ++NG+++GS+ A+ A+G TL Y IL + N AHG   TLGAY T+ +   TF
Sbjct: 1   MDISVFLQQLLNGLSIGSVYAIFALGYTLVYSILGIINLAHGAIFTLGAYFTYALMGGTF 60

Query: 58  GVN---------IWLSMIVAVV------GTVGVMLLSEKLLWSRMRSIRANSTTLIIISI 102
           G N         I L   VA++      G VGV +  E++ +  +R   +++   ++ S+
Sbjct: 61  GFNGLLANATLPIQLPFAVALIIGSSLAGLVGVAM--ERIAFQPLRKKGSDTLLTVVSSL 118

Query: 103 GLALFLRNGIILIWGGRNQNY------NLPITPALDIFG-----VKVPQNQLLVLALAVL 151
           G+A+ + N I  + G  +  +      NLP  PA + FG     + +   Q+++  ++V+
Sbjct: 119 GVAVVIVNIIQYLVGAESYTFPANTFGNLP--PAFN-FGTLEKPIPIRSVQVVIFTVSVV 175

Query: 152 SIGALHYLLQNTKIGKAMRAVADDLDLAKVSGIDVEQVIFWTWLIAGTVTSLGGSMY-GL 210
            +  L Y +  TK GKA++A+A+D   A + GI+ ++ I  T+ I+  +  L G++    
Sbjct: 176 IVAILTYFINCTKYGKAIQAIAEDATTASLLGINSDRFIVLTFFISSFLAGLAGTLVASS 235

Query: 211 ITAVRPNMGWFLILPLFASVILGGIGNPYGAIAAAFIIGIVQEVSTPFLGSQYKQGVALL 270
           ++   P  G    L   A ++LGG+G+  GA+    +IG+V E   P   S YK  VA  
Sbjct: 236 VSIAGPYFGIGFGLRGLAVIVLGGLGSIPGAVLGGLLIGVV-EALVPSDYSGYKDAVAFG 294

Query: 271 IMILVLLIRPKGL 283
           I+ ++LL+RP+GL
Sbjct: 295 ILFIMLLVRPQGL 307


Lambda     K      H
   0.328    0.144    0.426 

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: 273
Number of extensions: 16
Number of successful extensions: 4
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: 288
Length of database: 316
Length adjustment: 27
Effective length of query: 261
Effective length of database: 289
Effective search space:    75429
Effective search space used:    75429
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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