GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Bacteroides thetaiotaomicron VPI-5482

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate 351943 BT2415 aspartate aminotransferase (NCBI ptt file)

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__Btheta:351943
          Length = 397

 Score =  176 bits (446), Expect = 1e-48
 Identities = 117/370 (31%), Positives = 189/370 (51%), Gaps = 12/370 (3%)

Query: 30  QGEEILLLSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQRIAERHRRRSGQA 89
           QG +++ LSVG+PDF+TP  I +AA  ++    + Y+ V G  ALR  I E+ ++ +G  
Sbjct: 29  QGIDVINLSVGEPDFNTPDHIKEAAKKAIDDNFSRYSPVPGYPALRNAIVEKLKKENGLE 88

Query: 90  VDAEQVVVLAGAQCALYAVVQCLLNPGDEVIVAEPMYVTYEAVFGACGARVVPVPVRSEN 149
             A Q+    GA+ ++   +  L+NPGDEVIV  P +V+Y  +        V V    E 
Sbjct: 89  YTAAQISCANGAKQSVCNAILVLVNPGDEVIVPAPYWVSYPEMVKMAEGTPVIVSAGIEQ 148

Query: 150 GFRVQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMAH-DLWMISDEVYS 208
            F++  +++ A ITP+T+A+ L SP NP+G+   +     LA +   +  + +I+DE+Y 
Sbjct: 149 DFKITPKQLEAAITPKTKALILCSPSNPTGSVYSKEELAGLAAVLAKYPQVVVIADEIYE 208

Query: 209 ELLFDGEHVSPASLPGMADRTATLNSLSKSHAMTGWRVGWVVGPAALCAHLENLALCMLY 268
            + + G H S A  P M +RT  +N +SK++AMTGWR+G++ GP  +      L      
Sbjct: 209 HINYIGAHQSIAQFPEMKERTVIVNGVSKAYAMTGWRIGFIAGPEWIVKACNKLQGQYTS 268

Query: 269 GSPEFIQDAACTALEAPLPELEAMREAYRRRRDLVIECLADSPGLRPLRPDGGMFVMVDI 328
           G     Q AA  A       ++ M++A+ RRRDL+++   + PG     P G  ++    
Sbjct: 269 GPCSVSQKAAEAAYVGTQEPVKEMQKAFERRRDLIVKLAKEVPGFEVNVPQGAFYLFPKC 328

Query: 329 -----RPTG----LSAQAFADRLLDRHGVSVLAGEAFGPSAAGHIRLGLVLGAEPLREAC 379
                +  G     ++   A  LL+   V+ + G +FG  A   IR+      E + EA 
Sbjct: 329 SYFFGKSNGERKIENSDDLAMYLLEDAHVACVGGTSFG--APECIRMSYATSDENIVEAI 386

Query: 380 RRIALCAAEL 389
           RRI    A+L
Sbjct: 387 RRIKEALAKL 396


Lambda     K      H
   0.322    0.136    0.411 

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: 379
Number of extensions: 20
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: 393
Length of database: 397
Length adjustment: 31
Effective length of query: 362
Effective length of database: 366
Effective search space:   132492
Effective search space used:   132492
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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