GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ilvE in Sphingomonas indica Dd16

Align aromatic-amino-acid transaminase TyrB; EC 2.6.1.57 (characterized)
to candidate WP_085218430.1 B9N75_RS08650 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= CharProtDB::CH_004054
         (397 letters)



>NCBI__GCF_900177405.1:WP_085218430.1
          Length = 394

 Score =  219 bits (558), Expect = 1e-61
 Identities = 136/396 (34%), Positives = 203/396 (51%), Gaps = 9/396 (2%)

Query: 1   MFQKVDAYAGDPILTLMERFKEDPRSDKVNLSIGLYYNEDGIIPQLQAVAEAEARLNAQP 60
           MFQ +     D +  +M  F+ DPR  K++L +G+Y ++ G  P + AV  AEARL A  
Sbjct: 1   MFQTIPDPVPDALHGVMAAFRADPRPHKIDLGVGVYRDDSGASPVMAAVKAAEARLVAD- 59

Query: 61  HGASLYLPMEGLNCYRHAIAPLLFGADHPVLKQQRVATIQTLGGSGALKVGADFLKRYFP 120
             +  Y  ++G   +   +  L  G   P     R A IQ  GG+G L++  +  K   P
Sbjct: 60  QDSKAYQALKGDEAFVAGLGALALGVPLP----PRAAAIQGSGGTGCLRLALELAKAANP 115

Query: 121 ESGVWVSDPTWENHVAIFAGAGFEVSTYPWYDEATNGVRFNDLLATLKTLPARSIVLLHP 180
           E  + +  P+W NH  + A  G  + T+ ++D     +    + A  +   A  + L H 
Sbjct: 116 EVRLHLGLPSWPNHANLAAATGIALVTHRYFDVEAQRIDREAVRAAAEGTRAGDLFLFHG 175

Query: 181 CCHNPTGADLTNDQWDAVIEILKARELIPFLDIAYQGFGAGMEEDAYAIRAIASAGLPAL 240
            CHNPTG+DL +     ++ IL+    +P +D+AY G G G+E D   +R +A A   AL
Sbjct: 176 LCHNPTGSDLDDSDRAGLLAILRENGAVPLVDVAYYGLGDGLEADLAFVRTVA-AEPRAL 234

Query: 241 VSNSFSKIFSLYGERVGGLSVMCEDAEAAGRVLGQLKATVRRNYSSPPNFGAQVVAAVLN 300
           +S + SK F LY ER G L  + E    A RV G+L+   R   S PP  GA VV  +L 
Sbjct: 235 ISVACSKAFGLYRERTGLLIAVAESEAEAARVQGRLETISRTLVSMPPAHGAAVVVDILV 294

Query: 301 DEALKASWLAEVEEMRTRILAMRQELVKVLSTEMPERNFDYLLNQRGMFSYTGLSAAQVD 360
           D AL+  W+ E+EEMR RI  +R EL + LS   P      +  QRG+F    LS  Q+ 
Sbjct: 295 DSALRKDWMVELEEMRARIFGLRGEL-EALSNVAP--MLAGISRQRGIFRMLPLSPDQIA 351

Query: 361 RLREEFGVYLIASGRMCVAGLNTANVQRVAKAFAAV 396
            L  +  +++  SGR+ +AGL   +  R+A+A AA+
Sbjct: 352 ALARDHAIHMAPSGRINIAGLKAGDAARLAEALAAL 387


Lambda     K      H
   0.320    0.135    0.401 

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: 341
Number of extensions: 19
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: 397
Length of database: 394
Length adjustment: 31
Effective length of query: 366
Effective length of database: 363
Effective search space:   132858
Effective search space used:   132858
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