GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Halorhodospira halophila SL1

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_011814596.1 HHAL_RS09130 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000015585.1:WP_011814596.1
          Length = 356

 Score =  211 bits (538), Expect = 2e-59
 Identities = 151/341 (44%), Positives = 192/341 (56%), Gaps = 28/341 (8%)

Query: 1   MAYRICLIEGDGIGHEVIPAARRVLEAT----GLPLEFVEAEAGWETFERRGTSVPEETV 56
           MA +I L+ GDGIG E+   ARRVLEA     G+  E   A  G   ++  G  +P+ET+
Sbjct: 1   MAQKILLLPGDGIGPEITAEARRVLEALNKRYGVGCEMETAPIGGAGYDAAGQPLPDETL 60

Query: 57  EKILSCHATLFGAATSPT-----RKVPGFFGAIRYLRRRLDLYANVRPAKSRP-VPGSRP 110
                  A L GA   P      R V    G +  +R  L L+ N+RPA   P + G+  
Sbjct: 61  RLAREADAVLLGAVGGPQYDALPRDVRPERGLLA-IRSELGLFGNLRPAILYPQLAGASA 119

Query: 111 -------GVDLVIVRENTEGLYVEQER--RYLDVAIADA----VISKKASERIGRAALRI 157
                  G+D++IVRE T G+Y  Q R  R LD          V S+   ERI R A   
Sbjct: 120 LREDVVAGLDILIVRELTGGIYFGQPRGIRTLDSGERQGFNTEVYSESEIERIARLAFAA 179

Query: 158 AEGRPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERF 217
           AE R  +   +  KANVL  ++ L+ + V+ VA D+P V +  + VDN AMQLV  P++F
Sbjct: 180 AEQRQGRVCSV-DKANVLESSE-LWREVVERVAADYPGVELSHMYVDNAAMQLVRAPKQF 237

Query: 218 DVIVTTNLLGDILSDLAAGLVGGLGLAPSGNIGD-TTAVFEPVHGSAPDIAGKGIANPTA 276
           DV+VT NL GDILSD AA L G +G+ PS ++ +    ++EPVHGSAPDIAG+  ANP A
Sbjct: 238 DVVVTGNLFGDILSDCAAQLTGSIGMLPSASLDEHGKGLYEPVHGSAPDIAGQDKANPLA 297

Query: 277 AILSAAMMLDY-LGEKEAAKRVEKAVDLVLERGPRTPDLGG 316
            ILS AMML Y LG  EAA RVE AV  VLE G RTPDL G
Sbjct: 298 TILSVAMMLRYSLGAGEAADRVEAAVGAVLEEGLRTPDLQG 338


Lambda     K      H
   0.319    0.137    0.391 

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: 315
Number of extensions: 15
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: 334
Length of database: 356
Length adjustment: 29
Effective length of query: 305
Effective length of database: 327
Effective search space:    99735
Effective search space used:    99735
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 Jul 25 2024. The underlying query database was built on Jul 25 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