GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Amycolatopsis halophila YIM 93223

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_034277550.1 AMYHA_RS16255 carboxypeptidase regulatory-like domain-containing protein

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_000504245.1:WP_034277550.1
          Length = 449

 Score =  207 bits (527), Expect = 3e-58
 Identities = 115/283 (40%), Positives = 180/283 (63%), Gaps = 7/283 (2%)

Query: 6   IQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFVNTFGVNIWLSM 65
           +Q + NGI  G++IA++A+GL+L +G  RL NFAHG+ +T GA +  F +  G  + L  
Sbjct: 161 MQTLANGIQYGAVIAISAIGLSLVFGTTRLINFAHGELVTFGAVIALFFHVGGPGLPLIA 220

Query: 66  IVAVVGTVGVML--LSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILIWGGRNQNY 123
             A+    G +L    E+ LW  +R+       L IISIGLALFLR+ I++  G R ++Y
Sbjct: 221 AGAIAVVAGGLLGGTLERGLWRPLRNRGTGRINLFIISIGLALFLRHLILVFQGSRPESY 280

Query: 124 ---NLPITPALDIFGVKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMRAVADDLDLAK 180
              NL  T    +F +      +++++LAVL   A+ ++LQ T+IG A+RAV+D+ DLA 
Sbjct: 281 IDFNLQKTMDFGLFVITPRDLGIVLISLAVLF--AVAFMLQRTRIGTAIRAVSDNRDLAS 338

Query: 181 VSGIDVEQVIFWTWLIAGTVTSLGGSMYGLITAVRPNMGWFLILPLFASVILGGIGNPYG 240
            SGI+V QVI   W++ G + +LGG ++GL   V   MG+ L+L +FA +ILGG+G+ YG
Sbjct: 339 SSGINVNQVIMVVWVLGGGLAALGGVLFGLAQVVHWEMGFKLLLLMFAGIILGGLGSAYG 398

Query: 241 AIAAAFIIGIVQEVSTPFLGSQYKQGVALLIMILVLLIRPKGL 283
           A+  +F++GIV  +ST +  ++ +   ALL++I+VLL RP+G+
Sbjct: 399 AMVGSFVVGIVSHISTLWFPAELQNAWALLVLIIVLLFRPQGI 441


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: 345
Number of extensions: 15
Number of successful extensions: 3
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: 449
Length adjustment: 29
Effective length of query: 259
Effective length of database: 420
Effective search space:   108780
Effective search space used:   108780
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: 49 (23.5 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