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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HJB8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.688 |
CLV_MEL_PAP_1 | 186 | 192 | PF00089 | 0.532 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.552 |
CLV_PCSK_FUR_1 | 283 | 287 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 285 | 287 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 467 | 469 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.457 |
DEG_APCC_KENBOX_2 | 45 | 49 | PF00400 | 0.545 |
DOC_MAPK_HePTP_8 | 464 | 479 | PF00069 | 0.514 |
DOC_PP1_RVXF_1 | 418 | 424 | PF00149 | 0.423 |
DOC_PP2B_LxvP_1 | 222 | 225 | PF13499 | 0.677 |
DOC_PP2B_LxvP_1 | 449 | 452 | PF13499 | 0.591 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.639 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 196 | 205 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 382 | 388 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 422 | 437 | PF00022 | 0.392 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.663 |
LIG_BRCT_BRCA1_1 | 238 | 242 | PF00533 | 0.572 |
LIG_CtBP_PxDLS_1 | 219 | 223 | PF00389 | 0.537 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.630 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.613 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.700 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.421 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.572 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.676 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.585 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.680 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.547 |
LIG_LIR_Gen_1 | 138 | 148 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 56 | 63 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.567 |
LIG_SH2_CRK | 228 | 232 | PF00017 | 0.729 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.387 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.458 |
LIG_SH2_SRC | 119 | 122 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 228 | 232 | PF00017 | 0.684 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.679 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.599 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.423 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.534 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.682 |
LIG_SUMO_SIM_anti_2 | 349 | 354 | PF11976 | 0.499 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 349 | 354 | PF11976 | 0.579 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.549 |
LIG_TYR_ITIM | 392 | 397 | PF00017 | 0.423 |
LIG_WW_1 | 116 | 119 | PF00397 | 0.512 |
LIG_WW_1 | 225 | 228 | PF00397 | 0.691 |
MOD_CDK_SPK_2 | 41 | 46 | PF00069 | 0.549 |
MOD_CDK_SPxxK_3 | 259 | 266 | PF00069 | 0.686 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.649 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.652 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.683 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.667 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.609 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.615 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.572 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.731 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.666 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.605 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.603 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.574 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.656 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.528 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.619 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.549 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.516 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.725 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.663 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.784 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.515 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.598 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.542 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.772 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.633 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.680 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.608 |
MOD_GlcNHglycan | 249 | 253 | PF01048 | 0.619 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.574 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.389 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.609 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.415 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.676 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.472 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.691 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.517 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.530 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.692 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.671 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.577 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.631 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.668 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.574 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.623 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.564 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.575 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.687 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.651 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.563 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.606 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.657 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.760 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.672 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.533 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.473 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.550 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.650 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.630 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.678 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.685 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.468 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.525 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.545 |
MOD_NEK2_2 | 304 | 309 | PF00069 | 0.374 |
MOD_PIKK_1 | 485 | 491 | PF00454 | 0.482 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.645 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.540 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.527 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.687 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.598 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.628 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.550 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.519 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.755 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.566 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.566 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.683 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.658 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.535 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.560 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.572 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.695 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.641 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.586 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.554 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.605 |
MOD_SUMO_for_1 | 423 | 426 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 324 | 332 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 432 | 442 | PF00179 | 0.481 |
TRG_DiLeu_BaEn_2 | 311 | 317 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.688 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6J5 | Leptomonas seymouri | 39% | 89% |
A0A3Q8ICJ1 | Leishmania donovani | 58% | 100% |
A4HJX4 | Leishmania braziliensis | 96% | 95% |
A4I6R1 | Leishmania infantum | 59% | 100% |
E9B1T3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 97% |
Q4Q6C8 | Leishmania major | 59% | 100% |