GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisC in Hydrogenophaga taeniospiralis NBRC 102512

Align Histidinol-phosphate aminotransferase; EC 2.6.1.9; Imidazole acetol-phosphate transaminase (uncharacterized)
to candidate WP_068174047.1 HTA01S_RS17665 histidinol-phosphate aminotransferase family protein

Query= curated2:Q9RRM7
         (361 letters)



>NCBI__GCF_001592305.1:WP_068174047.1
          Length = 360

 Score =  335 bits (860), Expect = 9e-97
 Identities = 176/356 (49%), Positives = 227/356 (63%), Gaps = 10/356 (2%)

Query: 9   PGPSGVRQAVRDIPAYPFTPIDVPYKLDQNENPYDFPPELKQKAAERMLAHPWNRYPDLH 68
           P P  VR AV   P YPF+PID P KLDQNE+  DFP  LK  A +RM   PW+RY DLH
Sbjct: 4   PLPPPVRAAVLASPDYPFSPIDAPVKLDQNESFADFPAPLKALALQRMQQLPWHRYTDLH 63

Query: 69  ADTLRAAIAGYEGWDAAGVVITPGSNVLIKILTELGGIGQTVLTTDPTFSVYTLEAAMLG 128
           A+ L AAIA ++GW A+G V T GSNVLI +L +L  +G  VLT  P F++Y L+A++LG
Sbjct: 64  AEELTAAIARHDGWSASGTVATTGSNVLIALLVQLAALGGRVLTVKPNFALYALDASLLG 123

Query: 129 AELVLTPLNPDFSLPVEATLQALAAHAP--------GVFYVTQPHAPTGHSDRPEDVRRV 180
           A L   PL  D SL ++A + AL   A         GV Y+ +PHAPTG     +++ R+
Sbjct: 124 AALTEVPLRADHSLDMDALIAALGTDADTNAPAQPRGVIYLPRPHAPTGSLCELDELDRL 183

Query: 181 VEVADRLGWVTVIDEAYSQYAGTDYRELVRAGKHVLSLRTFSKAWGLAGVRAGYLLTNPE 240
                  GW+ VIDEAY  +  TD R L R   HV+ LRTFSKAWGLAG+R GY L + E
Sbjct: 184 ARACP--GWLLVIDEAYHHFTDTDARALARQHPHVVLLRTFSKAWGLAGLRLGYALASDE 241

Query: 241 LAGHLQKLVSAFTINFLTQAVIETALEHPEYMRERVAEAIAERGRIYAAVQGHPTCTIFP 300
           +A  L+KLV  F ++ L       ALEHP+Y+RERVA   +ER R++ A+Q HPT  + P
Sbjct: 242 VARQLRKLVPPFGVSVLQTVSALVALEHPDYLRERVAHTRSERERLFKALQRHPTWQVAP 301

Query: 301 SNTNFFLLKTPDADAAYRHLLEHGIVCRRQDKLRGLDGCLRIAVGTPAENDALIAA 356
           S+ NF L++TPDA  A+  LL  G++ RRQD L GL GCLR+ VG+  ENDA ++A
Sbjct: 302 SHANFLLVRTPDAARAHAELLAQGVLVRRQDSLHGLQGCLRVTVGSVRENDAFLSA 357


Lambda     K      H
   0.320    0.137    0.414 

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: 394
Number of extensions: 14
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: 361
Length of database: 360
Length adjustment: 29
Effective length of query: 332
Effective length of database: 331
Effective search space:   109892
Effective search space used:   109892
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 (21.8 bits)
S2: 49 (23.5 bits)

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

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