Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 31 |
NetGPI | no | yes: 0, no: 31 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 32 |
GO:0110165 | cellular anatomical entity | 1 | 32 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: Q4QHB2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 5 |
GO:0006862 | nucleotide transport | 6 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0015748 | organophosphate ester transport | 5 | 5 |
GO:0015931 | nucleobase-containing compound transport | 5 | 5 |
GO:0051179 | localization | 1 | 5 |
GO:0051234 | establishment of localization | 2 | 5 |
GO:0055085 | transmembrane transport | 2 | 5 |
GO:0071702 | organic substance transport | 4 | 5 |
GO:0071705 | nitrogen compound transport | 4 | 5 |
GO:0035352 | NAD transmembrane transport | 4 | 1 |
GO:0043132 | NAD transport | 7 | 1 |
GO:1901679 | nucleotide transmembrane transport | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0015215 | nucleotide transmembrane transporter activity | 4 | 1 |
GO:0015605 | organophosphate ester transmembrane transporter activity | 3 | 1 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0051724 | NAD transmembrane transporter activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.476 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.196 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.257 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.196 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.289 |
CLV_PCSK_PC7_1 | 341 | 347 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.310 |
DEG_APCC_DBOX_1 | 136 | 144 | PF00400 | 0.592 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.723 |
DEG_SCF_FBW7_1 | 328 | 335 | PF00400 | 0.487 |
DOC_CKS1_1 | 329 | 334 | PF01111 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 100 | 106 | PF00134 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 317 | 323 | PF00134 | 0.338 |
DOC_MAPK_MEF2A_6 | 189 | 197 | PF00069 | 0.445 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.306 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.765 |
LIG_14-3-3_CanoR_1 | 110 | 120 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 224 | 230 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 213 | 229 | PF00022 | 0.537 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.454 |
LIG_CtBP_PxDLS_1 | 103 | 107 | PF00389 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 284 | 292 | PF00928 | 0.443 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.535 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.307 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.301 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.449 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.668 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.578 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.364 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.277 |
LIG_IBAR_NPY_1 | 319 | 321 | PF08397 | 0.456 |
LIG_LIR_Apic_2 | 284 | 290 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 373 | 381 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 77 | 86 | PF02991 | 0.517 |
LIG_LIR_LC3C_4 | 235 | 239 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 213 | 217 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.512 |
LIG_LYPXL_SIV_4 | 320 | 328 | PF13949 | 0.480 |
LIG_Pex14_1 | 247 | 251 | PF04695 | 0.252 |
LIG_PTB_Apo_2 | 253 | 260 | PF02174 | 0.150 |
LIG_PTB_Phospho_1 | 253 | 259 | PF10480 | 0.150 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.352 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.351 |
LIG_SH2_SRC | 15 | 18 | PF00017 | 0.616 |
LIG_SH2_SRC | 374 | 377 | PF00017 | 0.235 |
LIG_SH2_STAP1 | 376 | 380 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.458 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.499 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.782 |
LIG_TYR_ITIM | 155 | 160 | PF00017 | 0.518 |
MOD_CDC14_SPxK_1 | 206 | 209 | PF00782 | 0.396 |
MOD_CDK_SPxK_1 | 203 | 209 | PF00069 | 0.396 |
MOD_CDK_SPxxK_3 | 203 | 210 | PF00069 | 0.405 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.492 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.502 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.419 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.308 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.312 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.766 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.743 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.256 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.400 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.238 |
MOD_GlcNHglycan | 260 | 264 | PF01048 | 0.590 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.250 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.340 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.574 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.496 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.367 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.280 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.491 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.734 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.574 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.344 |
MOD_N-GLC_2 | 361 | 363 | PF02516 | 0.422 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.545 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.715 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.339 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.309 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.325 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.240 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.611 |
MOD_NEK2_2 | 225 | 230 | PF00069 | 0.430 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.491 |
MOD_PKA_1 | 110 | 116 | PF00069 | 0.579 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.476 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.716 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.499 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.419 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.305 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.728 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.521 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.522 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.454 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.759 |
TRG_DiLeu_BaEn_4 | 62 | 68 | PF01217 | 0.729 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.245 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.490 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.323 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4V4 | Leptomonas seymouri | 24% | 100% |
A0A0N1I8S5 | Leptomonas seymouri | 30% | 100% |
A0A0N1IBB8 | Leptomonas seymouri | 23% | 81% |
A0A0N1IHK9 | Leptomonas seymouri | 65% | 100% |
A0A0S4JF45 | Bodo saltans | 29% | 95% |
A0A0S4JH99 | Bodo saltans | 43% | 77% |
A0A0S4JIT1 | Bodo saltans | 31% | 100% |
A0A1X0NN16 | Trypanosomatidae | 30% | 100% |
A0A1X0NQB5 | Trypanosomatidae | 53% | 100% |
A0A1X0P6Z0 | Trypanosomatidae | 26% | 97% |
A0A3Q8IC78 | Leishmania donovani | 90% | 99% |
A0A3Q8IS12 | Leishmania donovani | 30% | 100% |
A0A3R7L1P3 | Trypanosoma rangeli | 29% | 100% |
A0A3S7WUZ5 | Leishmania donovani | 25% | 87% |
A0A422NGL1 | Trypanosoma rangeli | 53% | 100% |
A0A422P0Q3 | Trypanosoma rangeli | 29% | 99% |
A1CWA4 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 25% | 100% |
A4H690 | Leishmania braziliensis | 81% | 96% |
A4H9K7 | Leishmania braziliensis | 25% | 85% |
A4HQI4 | Leishmania braziliensis | 29% | 100% |
A4HUL3 | Leishmania infantum | 90% | 99% |
A4HXX3 | Leishmania infantum | 26% | 87% |
A4RPU0 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 23% | 100% |
B0Y4J4 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 25% | 100% |
C9ZVP0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
C9ZZS9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 97% |
E9AHZ3 | Leishmania infantum | 30% | 100% |
E9ANB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
E9ARN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 87% |
E9AU97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q3TZX3 | Mus musculus | 24% | 100% |
Q4Q094 | Leishmania major | 30% | 100% |
Q4QDU2 | Leishmania major | 27% | 100% |
Q4WQC5 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 25% | 100% |
Q54VX4 | Dictyostelium discoideum | 21% | 100% |
Q9BSK2 | Homo sapiens | 24% | 100% |
V5BTU3 | Trypanosoma cruzi | 52% | 100% |
V5DDT9 | Trypanosoma cruzi | 29% | 100% |
V5DN72 | Trypanosoma cruzi | 29% | 99% |