GapMind for catabolism of small carbon sources

 

Alignments for a candidate for put1 in Methylosarcina fibrata AML-C10

Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88); Proline dehydrogenase (EC 1.5.5.2) (characterized)
to candidate WP_020563770.1 A3OW_RS0112455 bifunctional proline dehydrogenase/L-glutamate gamma-semialdehyde dehydrogenase PutA

Query= reanno::ANA3:7023590
         (1064 letters)



>NCBI__GCF_000372865.1:WP_020563770.1
          Length = 1037

 Score =  945 bits (2443), Expect = 0.0
 Identities = 514/1040 (49%), Positives = 686/1040 (65%), Gaps = 19/1040 (1%)

Query: 24   ELFKAVTDNYIVDEEQYLSELIKLVPSSDEAIERVTRRAHELVNKVRQFDKKGLMVGIDA 83
            +L  A+  +Y+ DE+  ++EL++ + + D         A  LV  VR   K      I+A
Sbjct: 8    DLRAAINRSYLTDEKVIVNELLRNIGTYDPL--GAGELAGTLVTAVRA--KSHRNTAIEA 63

Query: 84   FLQQYSLETQEGIILMCLAEALLRIPDAATADALIEDKLSGAKWDEHLSKSDSVLVNAST 143
            FL +Y L ++EG++LM +AEALLRIPD+ T D  +++KL+GA W+ HL +SDS+LV+ + 
Sbjct: 64   FLHEYQLNSREGVVLMGIAEALLRIPDSRTQDLFLQEKLTGADWNRHLLQSDSLLVHFTN 123

Query: 144  WGLMLTGKIV-KLDKKIDGTPSNLLSRLVNRLGEPVIRQAMMAAMKIMGKQFVLGRTMKE 202
              L  T +   +L  K    P  +    ++RLG P+IR A+  AM+ + +QFV    M E
Sbjct: 124  KALSFTSEFEHRLLSKEHWLP--VFEEALSRLGAPLIRTAVKQAMRYLAQQFVFADAMPE 181

Query: 203  ALKNSEDKRKLGYTHSYDMLGEAALTRKDAEKYFNDYANAITELGAQSYNENESPRPTIS 262
            AL+ SE+  +  +  S+DMLGEAA+T  DAE+Y+  Y +A+  L  +    +    P IS
Sbjct: 182  ALQISEEFPEERF--SFDMLGEAAVTAADAERYYQAYRHAVRTLAERENLADPQLNPGIS 239

Query: 263  IKLSALHPRYEVANEDRVLTELYDTVIRLIKLARGLNIGISIDAEEVDRLELSLKLFQKL 322
            IKLSAL PRYE     R + EL + +  L + AR   I +++DAEE +RL++SL +F  +
Sbjct: 240  IKLSALCPRYEPLQHRRAVGELSEKLRALAREARAAGIPMTVDAEESERLDMSLDVFAAV 299

Query: 323  FNADATKGWGLLGIVVQAYSKRALPVLVWLTRLAKEQGDEIPVRLVKGAYWDSELKWAQQ 382
            F+    KGW  LG+ VQAY KRALPVL WL  LA      +PVRLVKGAYWDSE+K AQ+
Sbjct: 300  FSHPDLKGWPGLGLAVQAYQKRALPVLRWLAALAASHRCRVPVRLVKGAYWDSEIKRAQE 359

Query: 383  AGEAAYPLYTRKAGTDVSYLACARYLLSDATRGAIYPQFASHNAQTVAAISDMAGDRN-- 440
             G A YP++T K+ TDVSYLACA YLLS  +    YPQFA+HNA TVAAI   AG  +  
Sbjct: 360  NGLAGYPVFTHKSMTDVSYLACAHYLLSKTSE--FYPQFATHNAHTVAAILQ-AGKHHPG 416

Query: 441  HEFQRLHGMGQELYDTILSEAGAKA-VRIYAPIGAHKDLLPYLVRRLLENGANTSFVHKL 499
            +EFQRLHGMG+ LY  +++ +  K   R+YAP+G +++LLPYLVRRLLENGANTSF++++
Sbjct: 417  YEFQRLHGMGERLYREVMAVSERKIPCRVYAPVGDYRELLPYLVRRLLENGANTSFINQI 476

Query: 500  VDPKTPIESLVVHPLKTLTGYKTLANN-KIVLPTDIFGSDRKNSKGLNMNIISEAEPFFA 558
              P+  +  LV  P++T+   K+L    +IVLP D++G  R NS G+N+    +      
Sbjct: 477  DHPEWSVAELVRDPVETV---KSLPKTPQIVLPKDLYGERRPNSHGVNLADPFQLRQLQQ 533

Query: 559  ALDKFKSTQWQAGPLVNGQTLTGEHKTVVSPFDTTQTVGQVAFADKAAIEQAVASADAAF 618
             LD    TQW A P        G  + VV+P D   TVG V  A+ A +E+A+  A  AF
Sbjct: 534  ELDALAGTQWTAMPSGRKPLQAGAGRPVVNPCDNRLTVGSVGMAEPADVERALEKASHAF 593

Query: 619  ATWTRTPVEVRASALQKLADLLEENREELIALCTREAGKSIQDGIDEVREAVDFCRYYAV 678
              W  +    RA  L++  DLLE++R EL++LC RE G++++D + EVREAVD+CRYYA 
Sbjct: 594  NDWRLSSAATRAGCLRRAGDLLEQHRSELVSLCCREGGRTLRDALAEVREAVDYCRYYAQ 653

Query: 679  QAKKLMSKPELLPGPTGELNELFLQGRGVFVCISPWNFPLAIFLGQVSAALAAGNTVVAK 738
             A++L ++P LLPGPTGE N L+  GRGVFVCISPWNFP+AIF+GQ++AALAAGNTV+AK
Sbjct: 654  SAEELFAEPMLLPGPTGEENRLYYYGRGVFVCISPWNFPIAIFIGQMTAALAAGNTVIAK 713

Query: 739  PAEQTSIIGYRAVQLAHQAGIPTDVLQYLPGTGATVGNALTADERIGGVCFTGSTGTAKL 798
            PA QT +     V+L HQAGIP  VLQ++P  G   G+ L AD R+ G+ FTGST TA+ 
Sbjct: 714  PASQTVLTAMLCVRLLHQAGIPEPVLQFVPAEGRLSGDLLVADPRVAGIAFTGSTDTAQW 773

Query: 799  INRTLANREGAIIPLIAETGGQNAMVVDSTSQPEQVVNDVVSSSFTSAGQRCSALRVLFL 858
            I+R LA +   +IPLIAETGGQN M+ DS++ PEQ+V DVV+S+F SAGQRCSALRVLF+
Sbjct: 774  IHRRLAQQHPMLIPLIAETGGQNVMIADSSALPEQLVQDVVASTFNSAGQRCSALRVLFV 833

Query: 859  QEDIADRVIDVLQGAMDELVIGNPSSVKTDVGPVIDATAKANLDAHIDHIKQVGKLIKQM 918
            Q+DIAD++I +L GAM EL +G+P    TDVGPVID  A   L  H++ +++  +++ Q+
Sbjct: 834  QQDIADKIIGMLIGAMQELALGDPGRYATDVGPVIDRAALKPLAEHVEKMREQARMLYQL 893

Query: 919  SLPAGTENGHFVSPTAVEIDSIKVLEKEHFGPILHVIRYKASELAHVIDEINSTGFGLTL 978
             L      G F  PT +EI S+  L  E FGPILHVIRY+  EL  VI  IN TG+GLTL
Sbjct: 894  PLTEALSYGSFFPPTLIEIASLSQLTHEVFGPILHVIRYRGPELDRVIAAINETGYGLTL 953

Query: 979  GIHSRNEGHALEVADKVNVGNVYINRNQIGAVVGVQPFGGQGLSGTGPKAGGPHYLTRFV 1038
            GIHSR E     +   V VGN+Y+NRN IGAVVGVQPFGG GLSGTGPKAGGP YL RF 
Sbjct: 954  GIHSRIEATVRAIRQGVRVGNIYVNRNMIGAVVGVQPFGGMGLSGTGPKAGGPDYLRRFA 1013

Query: 1039 TEKTRTNNITAIGGNATLLS 1058
             E+T   N  A+GGNA LL+
Sbjct: 1014 VEQTVATNTAAVGGNAGLLA 1033


Lambda     K      H
   0.317    0.133    0.377 

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: 2385
Number of extensions: 92
Number of successful extensions: 8
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: 1064
Length of database: 1037
Length adjustment: 45
Effective length of query: 1019
Effective length of database: 992
Effective search space:  1010848
Effective search space used:  1010848
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: 58 (26.9 bits)

This GapMind analysis is from Sep 24 2021. 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