Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Related structures:
AlphaFold database: Q4Q9M8
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 14 |
GO:0009987 | cellular process | 1 | 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 16 |
GO:0005515 | protein binding | 2 | 14 |
GO:0030544 | Hsp70 protein binding | 4 | 14 |
GO:0031072 | heat shock protein binding | 3 | 14 |
GO:0051879 | Hsp90 protein binding | 4 | 14 |
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0008270 | zinc ion binding | 6 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0046914 | transition metal ion binding | 5 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.387 |
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.563 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.495 |
CLV_PCSK_FUR_1 | 346 | 350 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.584 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.478 |
DEG_SPOP_SBC_1 | 125 | 129 | PF00917 | 0.297 |
DOC_CYCLIN_RxL_1 | 179 | 191 | PF00134 | 0.481 |
DOC_MAPK_gen_1 | 81 | 89 | PF00069 | 0.281 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.511 |
DOC_USP7_UBL2_3 | 242 | 246 | PF12436 | 0.396 |
DOC_USP7_UBL2_3 | 260 | 264 | PF12436 | 0.396 |
LIG_14-3-3_CanoR_1 | 295 | 304 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 3 | 13 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 318 | 326 | PF00244 | 0.499 |
LIG_Actin_WH2_2 | 231 | 248 | PF00022 | 0.357 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.556 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.407 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.564 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.435 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.345 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.550 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.470 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 327 | 334 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 43 | 51 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 67 | 78 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 7 | 14 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.420 |
LIG_RPA_C_Fungi | 199 | 211 | PF08784 | 0.314 |
LIG_RPA_C_Fungi | 278 | 290 | PF08784 | 0.561 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.303 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.281 |
LIG_SH2_NCK_1 | 110 | 114 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 45 | 49 | PF00017 | 0.366 |
LIG_SH2_SRC | 130 | 133 | PF00017 | 0.338 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.412 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.471 |
LIG_TRAF2_1 | 285 | 288 | PF00917 | 0.476 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.423 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.465 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.343 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.550 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.626 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.364 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.468 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.333 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.596 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.558 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.497 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.431 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.392 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.387 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.480 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.312 |
MOD_GlcNHglycan | 215 | 219 | PF01048 | 0.327 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.592 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.462 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.418 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.272 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.508 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.489 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.638 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.725 |
MOD_LATS_1 | 293 | 299 | PF00433 | 0.415 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.319 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.308 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.520 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.249 |
MOD_N-GLC_2 | 330 | 332 | PF02516 | 0.524 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.540 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.499 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.444 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.412 |
MOD_PKA_1 | 347 | 353 | PF00069 | 0.527 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.520 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.540 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.588 |
MOD_PKB_1 | 289 | 297 | PF00069 | 0.467 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.414 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.323 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.459 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.399 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.404 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.508 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.441 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.355 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.459 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.599 |
MOD_SUMO_rev_2 | 149 | 155 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 21 | 29 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_1 | 196 | 201 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 267 | 272 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.326 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 349 | 352 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.348 |
TRG_NLS_MonoExtC_3 | 346 | 351 | PF00514 | 0.496 |
TRG_NLS_MonoExtN_4 | 346 | 352 | PF00514 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.464 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBD2 | Leptomonas seymouri | 64% | 100% |
A0A0S4JRK3 | Bodo saltans | 33% | 100% |
A0A1X0NZH9 | Trypanosomatidae | 37% | 96% |
A0A3Q8IJP8 | Leishmania donovani | 24% | 100% |
A0A3R7LE97 | Trypanosoma rangeli | 40% | 99% |
A0A3S7WZC1 | Leishmania donovani | 95% | 100% |
A4HEB3 | Leishmania braziliensis | 82% | 98% |
A4I1Q9 | Leishmania infantum | 95% | 100% |
A4ICY0 | Leishmania infantum | 24% | 100% |
C9ZKB4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ASC5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AXU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q271 | Leishmania major | 24% | 100% |
V5BCJ3 | Trypanosoma cruzi | 40% | 99% |