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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4IBA4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.721 |
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.686 |
CLV_C14_Caspase3-7 | 438 | 442 | PF00656 | 0.740 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.739 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.822 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.761 |
CLV_PCSK_FUR_1 | 314 | 318 | PF00082 | 0.333 |
CLV_PCSK_FUR_1 | 6 | 10 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.760 |
CLV_PCSK_PC7_1 | 447 | 453 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.770 |
DOC_CKS1_1 | 392 | 397 | PF01111 | 0.691 |
DOC_CKS1_1 | 99 | 104 | PF01111 | 0.593 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 425 | 431 | PF00134 | 0.654 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.719 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.664 |
DOC_USP7_MATH_2 | 395 | 401 | PF00917 | 0.701 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 193 | 198 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 340 | 345 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 461 | 465 | PF00244 | 0.672 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.707 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.589 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.744 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.553 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.508 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.715 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.567 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.606 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.769 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.708 |
LIG_LIR_Apic_2 | 219 | 225 | PF02991 | 0.707 |
LIG_LIR_Apic_2 | 322 | 327 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 66 | 75 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.357 |
LIG_Pex14_2 | 266 | 270 | PF04695 | 0.567 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.533 |
LIG_SH2_NCK_1 | 324 | 328 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.629 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.507 |
LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.623 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.556 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.547 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.493 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.438 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.741 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.673 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.531 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.741 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.614 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.775 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.593 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.639 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.758 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.681 |
MOD_Cter_Amidation | 314 | 317 | PF01082 | 0.369 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.733 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.696 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.383 |
MOD_GlcNHglycan | 230 | 234 | PF01048 | 0.751 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.789 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.361 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.671 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.658 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.783 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.518 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.579 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.510 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.734 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.683 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.623 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.379 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.456 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.504 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.730 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.438 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.722 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.505 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.589 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.591 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.532 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.584 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.755 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.391 |
MOD_NEK2_2 | 345 | 350 | PF00069 | 0.503 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.533 |
MOD_PK_1 | 429 | 435 | PF00069 | 0.550 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.683 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.357 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.738 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.720 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.794 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.815 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.731 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.438 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.415 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.505 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.688 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.753 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.389 |
MOD_Plk_2-3 | 397 | 403 | PF00069 | 0.727 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.712 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.427 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.624 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.679 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.674 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.696 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.614 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.391 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.681 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.583 |
MOD_SUMO_rev_2 | 50 | 58 | PF00179 | 0.677 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.783 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.808 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZT1 | Leptomonas seymouri | 53% | 100% |
A0A0S4JH24 | Bodo saltans | 38% | 100% |
A0A3Q8IJ10 | Leishmania donovani | 99% | 100% |
A0A422NNS8 | Trypanosoma rangeli | 44% | 100% |
A4HMM6 | Leishmania braziliensis | 73% | 99% |
E9AF28 | Leishmania major | 91% | 100% |
E9B684 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |