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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H6F1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 205 | 209 | PF00656 | 0.404 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.527 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.577 |
CLV_PCSK_FUR_1 | 394 | 398 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.696 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.631 |
DEG_SPOP_SBC_1 | 236 | 240 | PF00917 | 0.685 |
DEG_SPOP_SBC_1 | 413 | 417 | PF00917 | 0.561 |
DOC_ANK_TNKS_1 | 169 | 176 | PF00023 | 0.537 |
DOC_CKS1_1 | 131 | 136 | PF01111 | 0.684 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.557 |
DOC_PP2B_LxvP_1 | 382 | 385 | PF13499 | 0.642 |
DOC_PP4_FxxP_1 | 346 | 349 | PF00568 | 0.405 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.521 |
DOC_USP7_UBL2_3 | 386 | 390 | PF12436 | 0.590 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.649 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.813 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 118 | 127 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 139 | 143 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 473 | 478 | PF00244 | 0.523 |
LIG_Actin_WH2_2 | 193 | 209 | PF00022 | 0.595 |
LIG_Actin_WH2_2 | 309 | 326 | PF00022 | 0.550 |
LIG_Actin_WH2_2 | 431 | 448 | PF00022 | 0.521 |
LIG_BIR_III_4 | 253 | 257 | PF00653 | 0.483 |
LIG_Clathr_ClatBox_1 | 266 | 270 | PF01394 | 0.667 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.716 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.446 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.625 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.446 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.461 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.643 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.572 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.614 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.574 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.608 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.532 |
LIG_GBD_Chelix_1 | 182 | 190 | PF00786 | 0.585 |
LIG_HP1_1 | 465 | 469 | PF01393 | 0.696 |
LIG_LIR_Apic_2 | 300 | 306 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 136 | 143 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 311 | 319 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 425 | 436 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 300 | 305 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.505 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.737 |
LIG_SH2_NCK_1 | 128 | 132 | PF00017 | 0.696 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.603 |
LIG_SH3_1 | 128 | 134 | PF00018 | 0.692 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.692 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.719 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.629 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.521 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 464 | 470 | PF11976 | 0.612 |
LIG_TRFH_1 | 259 | 263 | PF08558 | 0.494 |
LIG_TRFH_1 | 302 | 306 | PF08558 | 0.518 |
MOD_CDK_SPK_2 | 165 | 170 | PF00069 | 0.540 |
MOD_CDK_SPK_2 | 397 | 402 | PF00069 | 0.742 |
MOD_CDK_SPK_2 | 481 | 486 | PF00069 | 0.527 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.716 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.544 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.727 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.640 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.570 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.697 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.538 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.629 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.606 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.684 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.553 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.742 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.626 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.542 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.577 |
MOD_GlcNHglycan | 270 | 274 | PF01048 | 0.503 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.653 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.711 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.644 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.638 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.548 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.746 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.615 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.660 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.641 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.474 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.536 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.646 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.706 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.475 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.584 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.507 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.630 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.746 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.583 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.689 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.735 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.540 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.706 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.647 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.577 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.540 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.620 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.542 |
MOD_NEK2_2 | 202 | 207 | PF00069 | 0.572 |
MOD_PK_1 | 10 | 16 | PF00069 | 0.467 |
MOD_PKA_1 | 386 | 392 | PF00069 | 0.562 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.693 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.626 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.540 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.677 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.654 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.567 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.486 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.482 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.685 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.674 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.602 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.621 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.815 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.647 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.636 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.475 |
MOD_SUMO_for_1 | 392 | 395 | PF00179 | 0.562 |
TRG_AP2beta_CARGO_1 | 311 | 320 | PF09066 | 0.356 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.524 |
TRG_NLS_MonoExtC_3 | 385 | 390 | PF00514 | 0.647 |
TRG_NLS_MonoExtN_4 | 383 | 390 | PF00514 | 0.625 |
TRG_NLS_MonoExtN_4 | 6 | 13 | PF00514 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 338 | 343 | PF00026 | 0.465 |
TRG_PTS1 | 484 | 487 | PF00515 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBY1 | Leptomonas seymouri | 34% | 100% |
A0A3Q8I8Z9 | Leishmania donovani | 65% | 100% |
A4HUU5 | Leishmania infantum | 64% | 100% |
E9ANI0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 97% |
Q4QH46 | Leishmania major | 65% | 100% |