GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisC in Trichodesmium erythraeum IMS101

Align Histidinol-phosphate aminotransferase; EC 2.6.1.9; Imidazole acetol-phosphate transaminase (uncharacterized)
to candidate WP_044137258.1 TERY_RS07480 threonine-phosphate decarboxylase

Query= curated2:B0K625
         (351 letters)



>NCBI__GCF_000014265.1:WP_044137258.1
          Length = 356

 Score =  138 bits (348), Expect = 2e-37
 Identities = 102/333 (30%), Positives = 185/333 (55%), Gaps = 17/333 (5%)

Query: 29  ANETPFELPEEVIKNIQEIVKSSQVNVYPDPTAEKLKEELA-RYCGVVPTNIFVGNGSDE 87
           A+  P  LP+  I+ IQ  +  S++  YPDP  ++LK+ L+  +  +    I  GNG+ E
Sbjct: 29  ASINPLGLPDSAIQAIQTNI--SKLGAYPDPNYQELKKALSLAHPPLTSEWILPGNGAAE 86

Query: 88  IIHLIMLAFINKGDVVAYPHPSFAMY--SVYSKIAGAVEIPVRLREDYNYDVDSFIKVIE 145
           ++    L  ++K + V    P+F  Y  ++ +  A  +E P+++ E    ++      IE
Sbjct: 87  LLTWAALD-LSKLEAVYLLTPAFGDYRRALKTFTANVIECPLKVGESKLTELQEL--QIE 143

Query: 146 KYQPKLVFLCNPNNPTGSVIEREDIIKIIQKSNGIVVVDEAYFEFY----GNTIVDAINE 201
               K + L NP+NPTG ++E E I+  ++K  G+VVVDEA+ +F       ++V  + +
Sbjct: 144 IDTDKGLLLNNPHNPTGLLMEVETIVPFLEKF-GLVVVDEAFMDFLPPPQAQSLVPLVTK 202

Query: 202 FENLIVLRTLSKAFGLAGLRVGYAVANENILKYLNLVKSPYNINSLSQIIALKVLRTDVL 261
           F NL++LR+L+K + L GLR+GYA+++   L+     + P+ +N+L+   A  VL   V 
Sbjct: 203 FHNLVILRSLTKFYSLPGLRLGYAISHPERLRKWQKWRDPWPVNTLAIAAAQAVLEDQVF 262

Query: 262 KERI-NYILEERKRLIKELGKIPGVKVYPSKTNFILV-KFKDADYVYQGLLER-GILVRD 318
           +++  +++ + R +L + L ++PG++  P   NF+LV   K  D++   LL++  IL+RD
Sbjct: 263 QQQTWDWLADARPQLFQGLAELPGLQPCPGAANFLLVHSEKSVDWLQTTLLKKHRILIRD 322

Query: 319 FSKVEGL-EGALRITVSSCEANDYLINGLKELL 350
            S    L +   R+ V + E N  L++ L ++L
Sbjct: 323 GSSFPELGDRYFRVAVRTQEDNQKLVDALGQIL 355


Lambda     K      H
   0.319    0.140    0.393 

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: 271
Number of extensions: 22
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: 351
Length of database: 356
Length adjustment: 29
Effective length of query: 322
Effective length of database: 327
Effective search space:   105294
Effective search space used:   105294
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

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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