GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Derxia gummosa DSM 723

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_028313015.1 H566_RS0121225 citrate synthase

Query= reanno::pseudo6_N2E2:Pf6N2E2_6062
         (375 letters)



>NCBI__GCF_000482785.1:WP_028313015.1
          Length = 436

 Score =  179 bits (455), Expect = 1e-49
 Identities = 124/389 (31%), Positives = 195/389 (50%), Gaps = 26/389 (6%)

Query: 11  GLRGQVAGQTALSTVGQSGAGLTYRGYDVRDLAADAQFEEVAYLLLYGELPTQAQLDAYT 70
           G     + Q+A++ +      L YRGY +  LA    F E  YLLL GELP   Q D + 
Sbjct: 50  GFLSTASCQSAITYIDGDKGELLYRGYPIEQLATKCDFLETCYLLLNGELPNATQKDDFV 109

Query: 71  GKLRQLRDLPQALKEVLERIPADAHPMDVMRTGCSFLGNLEPEQ----DFSQQHDKTDRL 126
            ++ Q   + + +   L     DAHPM V+      +    P+     D  Q+     RL
Sbjct: 110 ARVTQHTMVNEQMHFFLRGFRRDAHPMAVLTGLVGAMSAFYPDSMNLNDAHQREISAIRL 169

Query: 127 LAAFPAIMCYWYRFSHQGQRIECVTDEVSIGGHFLHLLHGK-----KPSELHVKVMNVSL 181
           +A  P ++   Y++S  GQ      +++S   +F  ++        K +++ V+ ++   
Sbjct: 170 IAKLPTLVAMAYKYSI-GQPFIYPHNDLSYTANFTRMMFATPCEEYKVNDVLVRALDRIF 228

Query: 182 ILYAEHEFNASTFTARVCASTLSDLFSCITAAIGSLRGPLHGGANEAAMEMIERFSSPQE 241
           IL+A+HE NAST T R+CAS+ ++ F+ I A +  L GP HGGANEAA+ M+    + Q 
Sbjct: 229 ILHADHEQNASTSTVRLCASSGTNPFAAIAAGVACLWGPAHGGANEAALNMLYDIQA-QG 287

Query: 242 AIEGTLGMLAR-KDK-----IMGFGHAIYKDNDPRNEVIKGWSKKLADEVG--DTVLFPV 293
            +E     +A+ KDK     +MGFGH +YK+ DPR ++++    ++   +G  +  LF +
Sbjct: 288 GVEKIGEFVAKVKDKNSGVRLMGFGHRVYKNYDPRAKLMRETCHEVLGALGLENDPLFKL 347

Query: 294 SEAIDKTMWE-----QKKLFPNADFYHASAYHFMGIPTKLFTPIFVCSRLTGWAAHVFEQ 348
           + A++K   E     Q+KL+PN DFY       +GIP  LFT IF  +R  GW A + E 
Sbjct: 348 AMALEKIALEDDYFVQRKLYPNVDFYSGIVQKAIGIPVSLFTAIFALARTVGWIAQLNEM 407

Query: 349 RAN--NRIIRPSAEYTGVEQRKFVPIEQR 375
             +   +I RP   +TG   R    +  R
Sbjct: 408 ITDPEYKIGRPRQLFTGAVTRNVPDLSAR 436


Lambda     K      H
   0.321    0.135    0.406 

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: 17
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: 375
Length of database: 436
Length adjustment: 31
Effective length of query: 344
Effective length of database: 405
Effective search space:   139320
Effective search space used:   139320
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 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