GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Kyrpidia tusciae DSM 2912

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_123809439.1 BTUS_RS11380 acetylornithine transaminase

Query= reanno::pseudo1_N1B4:Pf1N1B4_3440
         (406 letters)



>NCBI__GCF_000092905.1:WP_123809439.1
          Length = 386

 Score =  319 bits (817), Expect = 1e-91
 Identities = 161/371 (43%), Positives = 227/371 (61%), Gaps = 4/371 (1%)

Query: 29  VRGAGSRVWDQSGRELIDFAGGIAVNVLGHAHPALVAALTEQANKLWHVSNVFTNEPALR 88
           VRG G  +WD  G + +DFA GIAV +LGH+HPA+  A+ +QA  L H SN+F     + 
Sbjct: 12  VRGEGVWLWDADGNQYLDFAAGIAVTILGHSHPAVAEAIADQARTLLHCSNLFYIPQQVE 71

Query: 89  LAHKLVDATFAERVFFCNSGAEANEAAFKLARRVAHDRFGTEKYEIVAALNSFHGRTLFT 148
           LA+ LV+ +  ++VFFCNSG EA+EAA KLARR A+     E+  ++   +SFHGRTL  
Sbjct: 72  LANWLVNHSALDQVFFCNSGTEASEAAIKLARRWAYHNGVPERSTVITLEHSFHGRTLGA 131

Query: 149 VNVGGQSKYSDGFGPKITGITHVPYNDLAALKAAVSDKTCAVVLEPIQGEGGVLPAELSY 208
           +    Q KY +GFGP + G+ HVP  D+ AL+ A+    CAV++E +QGEGGV+P    Y
Sbjct: 132 LTATAQPKYQEGFGPLLGGVRHVPVGDVKALEEALDGTVCAVMMEMVQGEGGVMPVPTDY 191

Query: 209 LQGARELCDAHNALLVFDEVQTGMGRSGKLFAYQHYGVTPDILTSAKSLGGGFPIAAMLT 268
           +Q  R LCD  N LLV DEVQTGMGR+G  FAY+ +GV PDI T AK L  G P+ A+L 
Sbjct: 192 VQEVRALCDRRNVLLVIDEVQTGMGRTGTFFAYEQFGVEPDICTLAKGLANGVPVGAVLA 251

Query: 269 TEDLAKHLVVGTHGTTYGGNPLACAVAEAVIDVINTPEVLNGVNAKHDKFKTRLEQIGEK 328
              +A+  V G+HG+T+GGNPLA   A A ++V+    +      +    + RL      
Sbjct: 252 KRPVAEAFVPGSHGSTFGGNPLAMRAALATVEVVEKERLWEKAARRGAYLRGRLANALGN 311

Query: 329 YGLFTEVRGLGLLLGCVLSDAWKGKAKDIFNAAEREGLMILQAGPDVIRFAPSLVVEDAD 388
           +  F E+RG+GL++G VL +     A  +  A  + GL++  AG + +R  P L+VE+ +
Sbjct: 312 HPHFREIRGMGLMIGVVLDEG----ASQVAEACLKRGLLVTVAGGNTVRLLPPLIVEEPE 367

Query: 389 IDAGLDRFERA 399
           ID  ++R   A
Sbjct: 368 IDMAVERLSAA 378


Lambda     K      H
   0.320    0.136    0.400 

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: 396
Number of extensions: 19
Number of successful extensions: 2
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: 406
Length of database: 386
Length adjustment: 31
Effective length of query: 375
Effective length of database: 355
Effective search space:   133125
Effective search space used:   133125
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: 50 (23.9 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