GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tpi in Haloglycomyces albus DSM 45210

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_025274821.1 HALAL_RS0115220 phosphoglycerate kinase

Query= BRENDA::P36204
         (654 letters)



>NCBI__GCF_000527155.1:WP_025274821.1
          Length = 398

 Score =  389 bits (999), Expect = e-112
 Identities = 203/386 (52%), Positives = 265/386 (68%), Gaps = 9/386 (2%)

Query: 11  LKGKRVIMRVDFNVPVKDGVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRPKGEPSPE 70
           + G+RV++R D NVP+    + DD R+RA  PTIK   + GA+V + SHLGRPKGEP P+
Sbjct: 12  VSGRRVLLRADLNVPLDGSTITDDGRVRAVAPTIKALADAGARVTVCSHLGRPKGEPDPQ 71

Query: 71  FSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGET-KNDPE 129
           +SLAPVA+RL E+L   V F    VGD+  +    L +G+VLLLEN RF+PGET KND +
Sbjct: 72  YSLAPVARRLGEVLESTVAFATDTVGDDADEKNAALDDGDVLLLENLRFNPGETSKNDTQ 131

Query: 130 LAKFWASLA---DIHVNDAFGTAHRAHASNVGIAQFIPSVAGFLMEKEIKFLSKVTYNPE 186
            A+F   LA   D++V+DAFG  HR HAS   +A  +P  AGFL+  E+  LS++T   +
Sbjct: 132 RAEFAGELAAYGDVYVDDAFGAVHRKHASVYDVATMLPHYAGFLISNEVSVLSRLTGGAD 191

Query: 187 KPYVVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLA 246
           KPYVV+LGGAKVSDK+ VI NL+ K D ++IGG M +TFL A G EVG+S +E+D+I+  
Sbjct: 192 KPYVVILGGAKVSDKLAVIENLLSKVDTLIIGGGMAYTFLAAEGHEVGNSLLEKDQIETC 251

Query: 247 KELLEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQ 306
           +  LE+A   GVE++LPVD   A +     E +VV   D IP   MGLDIGP++  +F  
Sbjct: 252 QRYLEEAARLGVELLLPVDVASAAEFSASAEPQVVTA-DSIPSDRMGLDIGPDSARVFAD 310

Query: 307 KLSDAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDSAAAVNKFGL- 365
           +++ A TV WNGPMGVFE  ++A+GTK VA    +L +  A TVVGGGDSAAAV   GL 
Sbjct: 311 RINTAATVFWNGPMGVFEFPEYAKGTKAVA---QSLVDSEAFTVVGGGDSAAAVRTLGLP 367

Query: 366 EDKFSHVSTGGGASLEFLEGKELPGI 391
           ED F H+STGGGASLE+LEGK LPG+
Sbjct: 368 EDDFGHISTGGGASLEYLEGKTLPGL 393


Lambda     K      H
   0.317    0.137    0.386 

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: 652
Number of extensions: 26
Number of successful extensions: 5
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: 654
Length of database: 398
Length adjustment: 34
Effective length of query: 620
Effective length of database: 364
Effective search space:   225680
Effective search space used:   225680
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. 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