GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Cupriavidus basilensis 4G11

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate RR42_RS35305 RR42_RS35305 aspartate aminotransferase

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__Cup4G11:RR42_RS35305
          Length = 401

 Score =  214 bits (545), Expect = 3e-60
 Identities = 128/373 (34%), Positives = 196/373 (52%), Gaps = 15/373 (4%)

Query: 31  GEEILLLSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQRIAERHRRRSGQAV 90
           G +++ L+ G+PDF+TPA I +AA  ++ AG T Y DV G   LR   A++ +R +G   
Sbjct: 30  GRDVIGLTAGEPDFETPAHIREAAWRAMQAGKTRYTDVGGTAELRHAAAQKFKRENGLDY 89

Query: 91  DAEQVVVLAGAQCALYAVVQCLLNPGDEVIVAEPMYVTYEAVFGACGARVVPVPVRSENG 150
            A +++V  GA+  ++  + C +  GDEVIV  P +V+Y  +    G   V V  ++ENG
Sbjct: 90  AASEIIVSTGAKQVIFNALMCTVQQGDEVIVPAPYWVSYPDITLFAGGVPVFVACQAENG 149

Query: 151 FRVQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMAH-DLWMISDEVYSE 209
           F++  EE+   I+ RTR + LNSP+NPSGA+  R    A+AE+   H  +W+++D++Y  
Sbjct: 150 FKLTPEELERAISARTRWLILNSPNNPSGAAYTRTELVAIAEVLERHPHVWVMTDDIYEH 209

Query: 210 LLFDGEH--VSPASLPGMADRTATLNSLSKSHAMTGWRVGWVVGPAALCAHLENLALCML 267
           L +DG        + P +  RT T+N +SK++AMTGWR+G+   PA L   +  L     
Sbjct: 210 LTYDGAAFVTLAQAAPSLKARTLTINGVSKAYAMTGWRIGYAGAPAPLIKAMVKLQSQST 269

Query: 268 YGSPEFIQDAACTALEAPLPELEAMREAYRRRRDLVIECLADSPGLRPLRPDGGMFVMVD 327
            G+    Q AA  AL+ P   + A +  ++ RRD V+  L    G+    P G  +V   
Sbjct: 270 SGANAVAQAAAIAALDGPQDFIAANKAVFQARRDRVVAALGQVDGIHCQAPAGAFYVFAS 329

Query: 328 IR-------PTG---LSAQAFADRLLDRHGVSVLAGEAFGPSAAGHIRLGLVLGAEPLRE 377
                    P G    S+  + + +LD   ++VL G A+G     H RL        L E
Sbjct: 330 CEALIGARTPHGSVIRSSDDWVNWVLDSQDLAVLQGSAYGVDT--HFRLSFAASMAQLDE 387

Query: 378 ACRRIALCAAELL 390
            CRRI   AA L+
Sbjct: 388 GCRRIEAAAAALI 400


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: 430
Number of extensions: 26
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: 393
Length of database: 401
Length adjustment: 31
Effective length of query: 362
Effective length of database: 370
Effective search space:   133940
Effective search space used:   133940
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.

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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