Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_079650143.1 B5X82_RS21075 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_900167915.1:WP_079650143.1 Length = 498 Score = 366 bits (940), Expect = e-106 Identities = 204/483 (42%), Positives = 290/483 (60%), Gaps = 12/483 (2%) Query: 24 INGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAKR 83 I+G+ A +G + + P G+ A++ D + AV A+ F G W Q+A A+R Sbjct: 18 IDGQSRPAANGGWIDSIDPATGQVWAQIPDGRADDVDAAVAAAKRAFR-GPWRQMAAAQR 76 Query: 84 KAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDEVA 143 A L + ADL+ +EELA++ET D GK I D+ + DIP AQ H+ A A DK++ E Sbjct: 77 AALLRKVADLVAPRLEELAVIETRDNGKIINDTRAGDIPAIAQMFHYWAGAADKIHGETI 136 Query: 144 PTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAIRI 203 + V REP+GVVG IVPWN P + K+G ALA GN+VV+KP+E + + + + Sbjct: 137 QVSPASVNYVQREPIGVVGIIVPWNSPGSVFAAKVGAALAAGNTVVVKPAETASCSILVL 196 Query: 204 AQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNMKR 263 A+L +AG P GV+NV+ G G G A+A H DV + FTGST A+ + + E+ +K Sbjct: 197 AELFEQAGFPPGVVNVVAGLGAEAGDAIAGHPDVGKISFTGSTLTARAITRRSAEA-IKP 255 Query: 264 IWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFN--QGEVCTAGSRLLVERSIKDKFLPM 321 + E GGKS NIVFADA DL AAA + FN G+ C AGSR+LV+R I D+ + Sbjct: 256 LSFELGGKSANIVFADA-DLDAAAIGVTTMGIFNGAAGQSCIAGSRILVQRPIYDEMIER 314 Query: 322 VVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGG-------KRT 374 +V+ + G + G+P+D + +G + +Q V SY++ G ++G + + GG Sbjct: 315 MVKIITGIRLGDPMDAASQMGPIALDRQFEKVKSYLDLGRQEGGEAVCGGLAGEAVFGAG 374 Query: 375 LEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIW 434 GG +V+PT+F G+ N R +EEIFGPV V+ FD AEEAVAIAND+ YGLA G+W Sbjct: 375 SPHAGGYFVQPTLFAGLDNRARTVREEIFGPVACVLPFDDAEEAVAIANDSNYGLACGLW 434 Query: 435 TSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATW 494 T+D+ +AH+ A A+ AG+VWVN Y PFGG+K SG GRD + +L Y + K+ W Sbjct: 435 TNDLKRAHRMAAAIEAGAVWVNTYRRLHWAVPFGGYKDSGYGRDSGMESLRGYQQTKSVW 494 Query: 495 IKL 497 I L Sbjct: 495 IDL 497 Lambda K H 0.316 0.132 0.390 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: 691 Number of extensions: 26 Number of successful extensions: 4 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: 497 Length of database: 498 Length adjustment: 34 Effective length of query: 463 Effective length of database: 464 Effective search space: 214832 Effective search space used: 214832 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: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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:
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